Canonical Allele Identifier: CA2504586046

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153346_44153347insCG , CM000669.2:g.44153346_44153347insCG	GRCh38
NC_000007.13:g.44192945_44192946insCG , CM000669.1:g.44192945_44192946insCG	GRCh37
NC_000007.12:g.44159470_44159471insCG	NCBI36
NG_008847.1:g.41077_41078insCG
NG_008847.2:g.49824_49825insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*160_*161insCG	ENSP00000379142.4:n.*160_*161insCG
ENST00000616242.5:c.162_163insCG	ENSP00000482149.2:p.Val55ArgfsTer2
ENST00000682635.1:n.648_649insCG
ENST00000345378.7:c.165_166insCG	ENSP00000223366.2:p.Val56ArgfsTer2
ENST00000403799.8:c.162_163insCG MANE Select	ENSP00000384247.3:p.Val55ArgfsTer2
ENST00000671824.1:c.162_163insCG	ENSP00000500264.1:p.Val55ArgfsTer2
ENST00000673284.1:c.162_163insCG	ENSP00000499852.1:p.Val55ArgfsTer2
ENST00000345378.6:c.165_166insCG	ENSP00000223366.2:p.Val56ArgfsTer2
ENST00000395796.7:c.159_160insCG	ENSP00000379142.3:p.Val54ArgfsTer2
ENST00000403799.7:c.162_163insCG	ENSP00000384247.3:p.Val55ArgfsTer2
ENST00000437084.1:c.162_163insCG	ENSP00000402840.1:p.Val55ArgfsTer2
ENST00000616242.4:c.159_160insCG	ENSP00000482149.1:p.Val54ArgfsTer2
NM_000162.3:c.162_163insCG	NP_000153.1:p.Val55ArgfsTer2
NM_033507.1:c.165_166insCG	NP_277042.1:p.Val56ArgfsTer2
NM_033508.1:c.159_160insCG	NP_277043.1:p.Val54ArgfsTer2
NM_000162.4:c.162_163insCG	NP_000153.1:p.Val55ArgfsTer2
NM_001354800.1:c.162_163insCG	NP_001341729.1:p.Val55ArgfsTer2
NM_033507.2:c.165_166insCG	NP_277042.1:p.Val56ArgfsTer2
NM_033508.2:c.159_160insCG	NP_277043.1:p.Val54ArgfsTer2
NM_000162.5:c.162_163insCG MANE Select	NP_000153.1:p.Val55ArgfsTer2
NM_033507.3:c.165_166insCG	NP_277042.1:p.Val56ArgfsTer2
NM_033508.3:c.159_160insCG	NP_277043.1:p.Val54ArgfsTer2