Canonical Allele Identifier: CA2682582531
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145874_44145875insAATCCATT , CM000669.2:g.44145874_44145875insAATCCATT GRCh38
NC_000007.13:g.44185473_44185474insAATCCATT , CM000669.1:g.44185473_44185474insAATCCATT GRCh37
NC_000007.12:g.44151998_44151999insAATCCATT NCBI36
NG_008847.1:g.48549_48550insAATGGATT
NG_008847.2:g.57296_57297insAATGGATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1018-145_*1018-144insAATGGATT ENSP00000379142.4:n.*1018-145_*1018-144insAATGGATT
ENST00000616242.5:c.*140-145_*140-144insAATGGATT ENSP00000482149.2:n.*140-145_*140-144insAATGGATT
ENST00000683378.1:n.246-145_246-144insAATGGATT
ENST00000336642.9:c.54-145_54-144insAATGGATT ENSP00000338009.5:n.54-145_54-144insAATGGATT
ENST00000345378.7:c.1023-145_1023-144insAATGGATT ENSP00000223366.2:n.1023-145_1023-144insAATGGATT
ENST00000403799.8:c.1020-145_1020-144insAATGGATT MANE Select ENSP00000384247.3:n.1020-145_1020-144insAATGGATT
ENST00000671824.1:c.1083-145_1083-144insAATGGATT ENSP00000500264.1:n.1083-145_1083-144insAATGGATT
ENST00000672743.1:n.31+34_31+35insAATGGATT
ENST00000673284.1:c.1020-145_1020-144insAATGGATT ENSP00000499852.1:n.1020-145_1020-144insAATGGATT
ENST00000336642.8:c.72-145_72-144insAATGGATT ENSP00000338009.4:n.72-145_72-144insAATGGATT
ENST00000345378.6:c.1023-145_1023-144insAATGGATT ENSP00000223366.2:n.1023-145_1023-144insAATGGATT
ENST00000395796.7:c.1017-145_1017-144insAATGGATT ENSP00000379142.3:n.1017-145_1017-144insAATGGATT
ENST00000403799.7:c.1020-145_1020-144insAATGGATT ENSP00000384247.3:n.1020-145_1020-144insAATGGATT
ENST00000437084.1:c.969-145_969-144insAATGGATT ENSP00000402840.1:n.969-145_969-144insAATGGATT
ENST00000459642.1:n.255_256insAATGGATT
ENST00000473353.1:n.318-145_318-144insAATGGATT
ENST00000616242.4:c.1017-145_1017-144insAATGGATT ENSP00000482149.1:n.1017-145_1017-144insAATGGATT
NM_000162.3:c.1020-145_1020-144insAATGGATT NP_000153.1:n.1020-145_1020-144insAATGGATT
NM_033507.1:c.1023-145_1023-144insAATGGATT NP_277042.1:n.1023-145_1023-144insAATGGATT
NM_033508.1:c.1017-145_1017-144insAATGGATT NP_277043.1:n.1017-145_1017-144insAATGGATT
NM_000162.4:c.1020-145_1020-144insAATGGATT NP_000153.1:n.1020-145_1020-144insAATGGATT
NM_001354800.1:c.1020-145_1020-144insAATGGATT NP_001341729.1:n.1020-145_1020-144insAATGGATT
NM_001354801.1:c.9-145_9-144insAATGGATT NP_001341730.1:n.9-145_9-144insAATGGATT
NM_001354802.1:c.-122+34_-122+35insAATGGATT NP_001341731.1:n.-122+34_-122+35insAATGGATT
NM_001354803.1:c.54-145_54-144insAATGGATT NP_001341732.1:n.54-145_54-144insAATGGATT
NM_033507.2:c.1023-145_1023-144insAATGGATT NP_277042.1:n.1023-145_1023-144insAATGGATT
NM_033508.2:c.1017-145_1017-144insAATGGATT NP_277043.1:n.1017-145_1017-144insAATGGATT
XM_024446707.1:c.-122+34_-122+35insAATGGATT XP_024302475.1:n.-122+34_-122+35insAATGGATT
NM_000162.5:c.1020-145_1020-144insAATGGATT MANE Select NP_000153.1:n.1020-145_1020-144insAATGGATT
NM_033507.3:c.1023-145_1023-144insAATGGATT NP_277042.1:n.1023-145_1023-144insAATGGATT
NM_033508.3:c.1017-145_1017-144insAATGGATT NP_277043.1:n.1017-145_1017-144insAATGGATT
NM_001354803.2:c.54-145_54-144insAATGGATT NP_001341732.1:n.54-145_54-144insAATGGATT