Canonical Allele Identifier: CA2682582624
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145893_44145895del , CM000669.2:g.44145893_44145895del GRCh38
NC_000007.13:g.44185492_44185494del , CM000669.1:g.44185492_44185494del GRCh37
NC_000007.12:g.44152017_44152019del NCBI36
NG_008847.1:g.48531_48533del
NG_008847.2:g.57278_57280del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1018-163_*1018-161del ENSP00000379142.4:n.*1018-163_*1018-161del
ENST00000616242.5:c.*140-163_*140-161del ENSP00000482149.2:n.*140-163_*140-161del
ENST00000683378.1:n.246-163_246-161del
ENST00000336642.9:c.54-163_54-161del ENSP00000338009.5:n.54-163_54-161del
ENST00000345378.7:c.1023-163_1023-161del ENSP00000223366.2:n.1023-163_1023-161del
ENST00000403799.8:c.1020-163_1020-161del MANE Select ENSP00000384247.3:n.1020-163_1020-161del
ENST00000671824.1:c.1083-163_1083-161del ENSP00000500264.1:n.1083-163_1083-161del
ENST00000672743.1:n.31+16_31+18del
ENST00000673284.1:c.1020-163_1020-161del ENSP00000499852.1:n.1020-163_1020-161del
ENST00000336642.8:c.72-163_72-161del ENSP00000338009.4:n.72-163_72-161del
ENST00000345378.6:c.1023-163_1023-161del ENSP00000223366.2:n.1023-163_1023-161del
ENST00000395796.7:c.1017-163_1017-161del ENSP00000379142.3:n.1017-163_1017-161del
ENST00000403799.7:c.1020-163_1020-161del ENSP00000384247.3:n.1020-163_1020-161del
ENST00000437084.1:c.969-163_969-161del ENSP00000402840.1:n.969-163_969-161del
ENST00000459642.1:n.237_239del
ENST00000473353.1:n.318-163_318-161del
ENST00000616242.4:c.1017-163_1017-161del ENSP00000482149.1:n.1017-163_1017-161del
NM_000162.3:c.1020-163_1020-161del NP_000153.1:n.1020-163_1020-161del
NM_033507.1:c.1023-163_1023-161del NP_277042.1:n.1023-163_1023-161del
NM_033508.1:c.1017-163_1017-161del NP_277043.1:n.1017-163_1017-161del
NM_000162.4:c.1020-163_1020-161del NP_000153.1:n.1020-163_1020-161del
NM_001354800.1:c.1020-163_1020-161del NP_001341729.1:n.1020-163_1020-161del
NM_001354801.1:c.9-163_9-161del NP_001341730.1:n.9-163_9-161del
NM_001354802.1:c.-122+16_-122+18del NP_001341731.1:n.-122+16_-122+18del
NM_001354803.1:c.54-163_54-161del NP_001341732.1:n.54-163_54-161del
NM_033507.2:c.1023-163_1023-161del NP_277042.1:n.1023-163_1023-161del
NM_033508.2:c.1017-163_1017-161del NP_277043.1:n.1017-163_1017-161del
XM_024446707.1:c.-122+16_-122+18del XP_024302475.1:n.-122+16_-122+18del
NM_000162.5:c.1020-163_1020-161del MANE Select NP_000153.1:n.1020-163_1020-161del
NM_033507.3:c.1023-163_1023-161del NP_277042.1:n.1023-163_1023-161del
NM_033508.3:c.1017-163_1017-161del NP_277043.1:n.1017-163_1017-161del
NM_001354803.2:c.54-163_54-161del NP_001341732.1:n.54-163_54-161del