Canonical Allele Identifier: CA2682585257

Gene: GCK

Linked Data

• gnomAD v4: 7-44146315-C-CTGGGACT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146315_44146316insTGGGACT , CM000669.2:g.44146315_44146316insTGGGACT	GRCh38
NC_000007.13:g.44185914_44185915insTGGGACT , CM000669.1:g.44185914_44185915insTGGGACT	GRCh37
NC_000007.12:g.44152439_44152440insTGGGACT	NCBI36
NG_008847.1:g.48108_48109insAGTCCCA
NG_008847.2:g.56855_56856insAGTCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+147_*1017+148insAGTCCCA	ENSP00000379142.4:n.*1017+147_*1017+148insAGTCCCA
ENST00000616242.5:c.*139+147_*139+148insAGTCCCA	ENSP00000482149.2:n.*139+147_*139+148insAGTCCCA
ENST00000683378.1:n.245+147_245+148insAGTCCCA
ENST00000345378.7:c.1022+147_1022+148insAGTCCCA	ENSP00000223366.2:n.1022+147_1022+148insAGTCCCA
ENST00000403799.8:c.1019+147_1019+148insAGTCCCA MANE Select	ENSP00000384247.3:n.1019+147_1019+148insAGTCCCA
ENST00000671824.1:c.1082+147_1082+148insAGTCCCA	ENSP00000500264.1:n.1082+147_1082+148insAGTCCCA
ENST00000673284.1:c.1019+147_1019+148insAGTCCCA	ENSP00000499852.1:n.1019+147_1019+148insAGTCCCA
ENST00000345378.6:c.1022+147_1022+148insAGTCCCA	ENSP00000223366.2:n.1022+147_1022+148insAGTCCCA
ENST00000395796.7:c.1016+147_1016+148insAGTCCCA	ENSP00000379142.3:n.1016+147_1016+148insAGTCCCA
ENST00000403799.7:c.1019+147_1019+148insAGTCCCA	ENSP00000384247.3:n.1019+147_1019+148insAGTCCCA
ENST00000437084.1:c.968+147_968+148insAGTCCCA	ENSP00000402840.1:n.968+147_968+148insAGTCCCA
ENST00000473353.1:n.317+147_317+148insAGTCCCA
ENST00000616242.4:c.1016+147_1016+148insAGTCCCA	ENSP00000482149.1:n.1016+147_1016+148insAGTCCCA
NM_000162.3:c.1019+147_1019+148insAGTCCCA	NP_000153.1:n.1019+147_1019+148insAGTCCCA
NM_033507.1:c.1022+147_1022+148insAGTCCCA	NP_277042.1:n.1022+147_1022+148insAGTCCCA
NM_033508.1:c.1016+147_1016+148insAGTCCCA	NP_277043.1:n.1016+147_1016+148insAGTCCCA
NM_000162.4:c.1019+147_1019+148insAGTCCCA	NP_000153.1:n.1019+147_1019+148insAGTCCCA
NM_001354800.1:c.1019+147_1019+148insAGTCCCA	NP_001341729.1:n.1019+147_1019+148insAGTCCCA
NM_001354801.1:c.8+303_8+304insAGTCCCA	NP_001341730.1:n.8+303_8+304insAGTCCCA
NM_033507.2:c.1022+147_1022+148insAGTCCCA	NP_277042.1:n.1022+147_1022+148insAGTCCCA
NM_033508.2:c.1016+147_1016+148insAGTCCCA	NP_277043.1:n.1016+147_1016+148insAGTCCCA
NM_000162.5:c.1019+147_1019+148insAGTCCCA MANE Select	NP_000153.1:n.1019+147_1019+148insAGTCCCA
NM_033507.3:c.1022+147_1022+148insAGTCCCA	NP_277042.1:n.1022+147_1022+148insAGTCCCA
NM_033508.3:c.1016+147_1016+148insAGTCCCA	NP_277043.1:n.1016+147_1016+148insAGTCCCA