Canonical Allele Identifier: CA2578878442
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145311del , CM000669.2:g.44145311del GRCh38
NC_000007.13:g.44184910del , CM000669.1:g.44184910del GRCh37
NC_000007.12:g.44151435del NCBI36
NG_008847.1:g.49115del
NG_008847.2:g.57862del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1252-29del ENSP00000379142.4:n.*1252-29del
ENST00000616242.5:c.*374-29del ENSP00000482149.2:n.*374-29del
ENST00000683378.1:n.480-29del
ENST00000336642.9:c.288-29del ENSP00000338009.5:n.288-29del
ENST00000345378.7:c.1257-29del ENSP00000223366.2:n.1257-29del
ENST00000403799.8:c.1254-29del MANE Select ENSP00000384247.3:n.1254-29del
ENST00000671824.1:c.1317-29del ENSP00000500264.1:n.1317-29del
ENST00000672743.1:n.266-29del
ENST00000673284.1:c.1254-29del ENSP00000499852.1:n.1254-29del
ENST00000336642.8:c.306-29del ENSP00000338009.4:n.306-29del
ENST00000345378.6:c.1257-29del ENSP00000223366.2:n.1257-29del
ENST00000395796.7:c.1251-29del ENSP00000379142.3:n.1251-29del
ENST00000403799.7:c.1254-29del ENSP00000384247.3:n.1254-29del
ENST00000437084.1:c.1203-29del ENSP00000402840.1:n.1203-29del
ENST00000459642.1:n.634-29del
ENST00000616242.4:c.1251-29del ENSP00000482149.1:n.1251-29del
NM_000162.3:c.1254-29del NP_000153.1:n.1254-29del
NM_033507.1:c.1257-29del NP_277042.1:n.1257-29del
NM_033508.1:c.1251-29del NP_277043.1:n.1251-29del
NM_000162.4:c.1254-29del NP_000153.1:n.1254-29del
NM_001354800.1:c.1254-29del NP_001341729.1:n.1254-29del
NM_001354801.1:c.243-29del NP_001341730.1:n.243-29del
NM_001354802.1:c.114-29del NP_001341731.1:n.114-29del
NM_001354803.1:c.288-29del NP_001341732.1:n.288-29del
NM_033507.2:c.1257-29del NP_277042.1:n.1257-29del
NM_033508.2:c.1251-29del NP_277043.1:n.1251-29del
XM_024446707.1:c.114-29del XP_024302475.1:n.114-29del
NM_000162.5:c.1254-29del MANE Select NP_000153.1:n.1254-29del
NM_033507.3:c.1257-29del NP_277042.1:n.1257-29del
NM_033508.3:c.1251-29del NP_277043.1:n.1251-29del
NM_001354803.2:c.288-29del NP_001341732.1:n.288-29del