Canonical Allele Identifier: CA1703634818

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147582_44147586delinsCGGCT , CM000669.2:g.44147582_44147586delinsCGGCT	GRCh38
NC_000007.13:g.44187181_44187185delinsCGGCT , CM000669.1:g.44187181_44187185delinsCGGCT	GRCh37
NC_000007.12:g.44153706_44153710delinsCGGCT	NCBI36
NG_008847.1:g.46838_46842delinsAGCCG
NG_008847.2:g.55585_55589delinsAGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*861+64_*861+68delinsAGCCG	ENSP00000379142.4:n.*861+64_*861+68delinsAGCCG
ENST00000616242.5:c.853+74_853+78delinsAGCCG	ENSP00000482149.2:n.853+74_853+78delinsAGCCG
ENST00000345378.7:c.866+64_866+68delinsAGCCG	ENSP00000223366.2:n.866+64_866+68delinsAGCCG
ENST00000403799.8:c.863+64_863+68delinsAGCCG MANE Select	ENSP00000384247.3:n.863+64_863+68delinsAGCCG
ENST00000671824.1:c.853+74_853+78delinsAGCCG	ENSP00000500264.1:n.853+74_853+78delinsAGCCG
ENST00000673284.1:c.863+64_863+68delinsAGCCG	ENSP00000499852.1:n.863+64_863+68delinsAGCCG
ENST00000345378.6:c.866+64_866+68delinsAGCCG	ENSP00000223366.2:n.866+64_866+68delinsAGCCG
ENST00000395796.7:c.860+64_860+68delinsAGCCG	ENSP00000379142.3:n.860+64_860+68delinsAGCCG
ENST00000403799.7:c.863+64_863+68delinsAGCCG	ENSP00000384247.3:n.863+64_863+68delinsAGCCG
ENST00000437084.1:c.812+64_812+68delinsAGCCG	ENSP00000402840.1:n.812+64_812+68delinsAGCCG
ENST00000616242.4:c.860+64_860+68delinsAGCCG	ENSP00000482149.1:n.860+64_860+68delinsAGCCG
NM_000162.3:c.863+64_863+68delinsAGCCG	NP_000153.1:n.863+64_863+68delinsAGCCG
NM_033507.1:c.866+64_866+68delinsAGCCG	NP_277042.1:n.866+64_866+68delinsAGCCG
NM_033508.1:c.860+64_860+68delinsAGCCG	NP_277043.1:n.860+64_860+68delinsAGCCG
NM_000162.4:c.863+64_863+68delinsAGCCG	NP_000153.1:n.863+64_863+68delinsAGCCG
NM_001354800.1:c.863+64_863+68delinsAGCCG	NP_001341729.1:n.863+64_863+68delinsAGCCG
NM_033507.2:c.866+64_866+68delinsAGCCG	NP_277042.1:n.866+64_866+68delinsAGCCG
NM_033508.2:c.860+64_860+68delinsAGCCG	NP_277043.1:n.860+64_860+68delinsAGCCG
NM_000162.5:c.863+64_863+68delinsAGCCG MANE Select	NP_000153.1:n.863+64_863+68delinsAGCCG
NM_033507.3:c.866+64_866+68delinsAGCCG	NP_277042.1:n.866+64_866+68delinsAGCCG
NM_033508.3:c.860+64_860+68delinsAGCCG	NP_277043.1:n.860+64_860+68delinsAGCCG