Canonical Allele Identifier: CA2740837471
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145323_44145324insCCC , CM000669.2:g.44145323_44145324insCCC GRCh38
NC_000007.13:g.44184922_44184923insCCC , CM000669.1:g.44184922_44184923insCCC GRCh37
NC_000007.12:g.44151447_44151448insCCC NCBI36
NG_008847.1:g.49101_49102insGGG
NG_008847.2:g.57848_57849insGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1252-43_*1252-42insGGG ENSP00000379142.4:n.*1252-43_*1252-42insGGG
ENST00000616242.5:c.*374-43_*374-42insGGG ENSP00000482149.2:n.*374-43_*374-42insGGG
ENST00000683378.1:n.480-43_480-42insGGG
ENST00000336642.9:c.288-43_288-42insGGG ENSP00000338009.5:n.288-43_288-42insGGG
ENST00000345378.7:c.1257-43_1257-42insGGG ENSP00000223366.2:n.1257-43_1257-42insGGG
ENST00000403799.8:c.1254-43_1254-42insGGG MANE Select ENSP00000384247.3:n.1254-43_1254-42insGGG
ENST00000671824.1:c.1317-43_1317-42insGGG ENSP00000500264.1:n.1317-43_1317-42insGGG
ENST00000672743.1:n.266-43_266-42insGGG
ENST00000673284.1:c.1254-43_1254-42insGGG ENSP00000499852.1:n.1254-43_1254-42insGGG
ENST00000336642.8:c.306-43_306-42insGGG ENSP00000338009.4:n.306-43_306-42insGGG
ENST00000345378.6:c.1257-43_1257-42insGGG ENSP00000223366.2:n.1257-43_1257-42insGGG
ENST00000395796.7:c.1251-43_1251-42insGGG ENSP00000379142.3:n.1251-43_1251-42insGGG
ENST00000403799.7:c.1254-43_1254-42insGGG ENSP00000384247.3:n.1254-43_1254-42insGGG
ENST00000437084.1:c.1203-43_1203-42insGGG ENSP00000402840.1:n.1203-43_1203-42insGGG
ENST00000459642.1:n.634-43_634-42insGGG
ENST00000616242.4:c.1251-43_1251-42insGGG ENSP00000482149.1:n.1251-43_1251-42insGGG
NM_000162.3:c.1254-43_1254-42insGGG NP_000153.1:n.1254-43_1254-42insGGG
NM_033507.1:c.1257-43_1257-42insGGG NP_277042.1:n.1257-43_1257-42insGGG
NM_033508.1:c.1251-43_1251-42insGGG NP_277043.1:n.1251-43_1251-42insGGG
NM_000162.4:c.1254-43_1254-42insGGG NP_000153.1:n.1254-43_1254-42insGGG
NM_001354800.1:c.1254-43_1254-42insGGG NP_001341729.1:n.1254-43_1254-42insGGG
NM_001354801.1:c.243-43_243-42insGGG NP_001341730.1:n.243-43_243-42insGGG
NM_001354802.1:c.114-43_114-42insGGG NP_001341731.1:n.114-43_114-42insGGG
NM_001354803.1:c.288-43_288-42insGGG NP_001341732.1:n.288-43_288-42insGGG
NM_033507.2:c.1257-43_1257-42insGGG NP_277042.1:n.1257-43_1257-42insGGG
NM_033508.2:c.1251-43_1251-42insGGG NP_277043.1:n.1251-43_1251-42insGGG
XM_024446707.1:c.114-43_114-42insGGG XP_024302475.1:n.114-43_114-42insGGG
NM_000162.5:c.1254-43_1254-42insGGG MANE Select NP_000153.1:n.1254-43_1254-42insGGG
NM_033507.3:c.1257-43_1257-42insGGG NP_277042.1:n.1257-43_1257-42insGGG
NM_033508.3:c.1251-43_1251-42insGGG NP_277043.1:n.1251-43_1251-42insGGG
NM_001354803.2:c.288-43_288-42insGGG NP_001341732.1:n.288-43_288-42insGGG