Canonical Allele Identifier: CA2695203097

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147743dup , CM000669.2:g.44147743dup	GRCh38
NC_000007.13:g.44187342dup , CM000669.1:g.44187342dup	GRCh37
NC_000007.12:g.44153867dup	NCBI36
NG_008847.1:g.46684dup
NG_008847.2:g.55431dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*771dup	ENSP00000379142.4:n.*771dup
ENST00000616242.5:c.773dup	ENSP00000482149.2:p.Ala259ArgfsTer16
ENST00000345378.7:c.776dup	ENSP00000223366.2:p.Ala260ArgfsTer16
ENST00000403799.8:c.773dup MANE Select	ENSP00000384247.3:p.Ala259ArgfsTer16
ENST00000671824.1:c.773dup	ENSP00000500264.1:p.Ala259ArgfsTer16
ENST00000673284.1:c.773dup	ENSP00000499852.1:p.Ala259ArgfsTer16
ENST00000345378.6:c.776dup	ENSP00000223366.2:p.Ala260ArgfsTer16
ENST00000395796.7:c.770dup	ENSP00000379142.3:p.Ala258ArgfsTer16
ENST00000403799.7:c.773dup	ENSP00000384247.3:p.Ala259ArgfsTer16
ENST00000437084.1:c.722dup	ENSP00000402840.1:p.Ala242ArgfsTer16
ENST00000616242.4:c.770dup	ENSP00000482149.1:p.Ala258ArgfsTer16
NM_000162.3:c.773dup	NP_000153.1:p.Ala259ArgfsTer16
NM_033507.1:c.776dup	NP_277042.1:p.Ala260ArgfsTer16
NM_033508.1:c.770dup	NP_277043.1:p.Ala258ArgfsTer16
XR_927223.1:n.77dup
NM_000162.4:c.773dup	NP_000153.1:p.Ala259ArgfsTer16
NM_001354800.1:c.773dup	NP_001341729.1:p.Ala259ArgfsTer16
NM_033507.2:c.776dup	NP_277042.1:p.Ala260ArgfsTer16
NM_033508.2:c.770dup	NP_277043.1:p.Ala258ArgfsTer16
XR_927223.2:n.77dup
NM_000162.5:c.773dup MANE Select	NP_000153.1:p.Ala259ArgfsTer16
NM_033507.3:c.776dup	NP_277042.1:p.Ala260ArgfsTer16
NM_033508.3:c.770dup	NP_277043.1:p.Ala258ArgfsTer16