Canonical Allele Identifier: CA1703613441

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146445_44146448delinsCCCT , CM000669.2:g.44146445_44146448delinsCCCT	GRCh38
NC_000007.13:g.44186044_44186047delinsCCCT , CM000669.1:g.44186044_44186047delinsCCCT	GRCh37
NC_000007.12:g.44152569_44152572delinsCCCT	NCBI36
NG_008847.1:g.47976_47979delinsAGGG
NG_008847.2:g.56723_56726delinsAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+15_*1017+18delinsAGGG	ENSP00000379142.4:n.*1017+15_*1017+18delinsAGGG
ENST00000616242.5:c.*139+15_*139+18delinsAGGG	ENSP00000482149.2:n.*139+15_*139+18delinsAGGG
ENST00000683378.1:n.245+15_245+18delinsAGGG
ENST00000345378.7:c.1022+15_1022+18delinsAGGG	ENSP00000223366.2:n.1022+15_1022+18delinsAGGG
ENST00000403799.8:c.1019+15_1019+18delinsAGGG MANE Select	ENSP00000384247.3:n.1019+15_1019+18delinsAGGG
ENST00000671824.1:c.1082+15_1082+18delinsAGGG	ENSP00000500264.1:n.1082+15_1082+18delinsAGGG
ENST00000673284.1:c.1019+15_1019+18delinsAGGG	ENSP00000499852.1:n.1019+15_1019+18delinsAGGG
ENST00000345378.6:c.1022+15_1022+18delinsAGGG	ENSP00000223366.2:n.1022+15_1022+18delinsAGGG
ENST00000395796.7:c.1016+15_1016+18delinsAGGG	ENSP00000379142.3:n.1016+15_1016+18delinsAGGG
ENST00000403799.7:c.1019+15_1019+18delinsAGGG	ENSP00000384247.3:n.1019+15_1019+18delinsAGGG
ENST00000437084.1:c.968+15_968+18delinsAGGG	ENSP00000402840.1:n.968+15_968+18delinsAGGG
ENST00000473353.1:n.317+15_317+18delinsAGGG
ENST00000616242.4:c.1016+15_1016+18delinsAGGG	ENSP00000482149.1:n.1016+15_1016+18delinsAGGG
NM_000162.3:c.1019+15_1019+18delinsAGGG	NP_000153.1:n.1019+15_1019+18delinsAGGG
NM_033507.1:c.1022+15_1022+18delinsAGGG	NP_277042.1:n.1022+15_1022+18delinsAGGG
NM_033508.1:c.1016+15_1016+18delinsAGGG	NP_277043.1:n.1016+15_1016+18delinsAGGG
NM_000162.4:c.1019+15_1019+18delinsAGGG	NP_000153.1:n.1019+15_1019+18delinsAGGG
NM_001354800.1:c.1019+15_1019+18delinsAGGG	NP_001341729.1:n.1019+15_1019+18delinsAGGG
NM_001354801.1:c.8+171_8+174delinsAGGG	NP_001341730.1:n.8+171_8+174delinsAGGG
NM_033507.2:c.1022+15_1022+18delinsAGGG	NP_277042.1:n.1022+15_1022+18delinsAGGG
NM_033508.2:c.1016+15_1016+18delinsAGGG	NP_277043.1:n.1016+15_1016+18delinsAGGG
NM_000162.5:c.1019+15_1019+18delinsAGGG MANE Select	NP_000153.1:n.1019+15_1019+18delinsAGGG
NM_033507.3:c.1022+15_1022+18delinsAGGG	NP_277042.1:n.1022+15_1022+18delinsAGGG
NM_033508.3:c.1016+15_1016+18delinsAGGG	NP_277043.1:n.1016+15_1016+18delinsAGGG