Canonical Allele Identifier: CA1703613354

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146300_44146305delinsTGCCCC , CM000669.2:g.44146300_44146305delinsTGCCCC	GRCh38
NC_000007.13:g.44185899_44185904delinsTGCCCC , CM000669.1:g.44185899_44185904delinsTGCCCC	GRCh37
NC_000007.12:g.44152424_44152429delinsTGCCCC	NCBI36
NG_008847.1:g.48119_48124delinsGGGGCA
NG_008847.2:g.56866_56871delinsGGGGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+158_*1017+163delinsGGGGCA	ENSP00000379142.4:n.*1017+158_*1017+163delinsGGGGCA
ENST00000616242.5:c.*139+158_*139+163delinsGGGGCA	ENSP00000482149.2:n.*139+158_*139+163delinsGGGGCA
ENST00000683378.1:n.245+158_245+163delinsGGGGCA
ENST00000345378.7:c.1022+158_1022+163delinsGGGGCA	ENSP00000223366.2:n.1022+158_1022+163delinsGGGGCA
ENST00000403799.8:c.1019+158_1019+163delinsGGGGCA MANE Select	ENSP00000384247.3:n.1019+158_1019+163delinsGGGGCA
ENST00000671824.1:c.1082+158_1082+163delinsGGGGCA	ENSP00000500264.1:n.1082+158_1082+163delinsGGGGCA
ENST00000673284.1:c.1019+158_1019+163delinsGGGGCA	ENSP00000499852.1:n.1019+158_1019+163delinsGGGGCA
ENST00000345378.6:c.1022+158_1022+163delinsGGGGCA	ENSP00000223366.2:n.1022+158_1022+163delinsGGGGCA
ENST00000395796.7:c.1016+158_1016+163delinsGGGGCA	ENSP00000379142.3:n.1016+158_1016+163delinsGGGGCA
ENST00000403799.7:c.1019+158_1019+163delinsGGGGCA	ENSP00000384247.3:n.1019+158_1019+163delinsGGGGCA
ENST00000437084.1:c.968+158_968+163delinsGGGGCA	ENSP00000402840.1:n.968+158_968+163delinsGGGGCA
ENST00000473353.1:n.317+158_317+163delinsGGGGCA
ENST00000616242.4:c.1016+158_1016+163delinsGGGGCA	ENSP00000482149.1:n.1016+158_1016+163delinsGGGGCA
NM_000162.3:c.1019+158_1019+163delinsGGGGCA	NP_000153.1:n.1019+158_1019+163delinsGGGGCA
NM_033507.1:c.1022+158_1022+163delinsGGGGCA	NP_277042.1:n.1022+158_1022+163delinsGGGGCA
NM_033508.1:c.1016+158_1016+163delinsGGGGCA	NP_277043.1:n.1016+158_1016+163delinsGGGGCA
NM_000162.4:c.1019+158_1019+163delinsGGGGCA	NP_000153.1:n.1019+158_1019+163delinsGGGGCA
NM_001354800.1:c.1019+158_1019+163delinsGGGGCA	NP_001341729.1:n.1019+158_1019+163delinsGGGGCA
NM_001354801.1:c.8+314_8+319delinsGGGGCA	NP_001341730.1:n.8+314_8+319delinsGGGGCA
NM_033507.2:c.1022+158_1022+163delinsGGGGCA	NP_277042.1:n.1022+158_1022+163delinsGGGGCA
NM_033508.2:c.1016+158_1016+163delinsGGGGCA	NP_277043.1:n.1016+158_1016+163delinsGGGGCA
NM_000162.5:c.1019+158_1019+163delinsGGGGCA MANE Select	NP_000153.1:n.1019+158_1019+163delinsGGGGCA
NM_033507.3:c.1022+158_1022+163delinsGGGGCA	NP_277042.1:n.1022+158_1022+163delinsGGGGCA
NM_033508.3:c.1016+158_1016+163delinsGGGGCA	NP_277043.1:n.1016+158_1016+163delinsGGGGCA