Canonical Allele Identifier: CA157884762

Gene: GCK

Linked Data

• ClinVar Variation Id: 910637
• ClinVar RCV Id: RCV001162558 ; RCV001162559 ; RCV001162560 ; RCV001162561 ; RCV002463782
• dbSNP Id: rs757266656
• gnomAD v4: 7-44189409-C-T
• MyVariant Identifiers: chr7:g.44229008C>T (hg19) ; chr7:g.44189409C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189409C>T , CM000669.2:g.44189409C>T	GRCh38
NC_000007.13:g.44229008C>T , CM000669.1:g.44229008C>T	GRCh37
NC_000007.12:g.44195533C>T	NCBI36
NG_008847.1:g.5015G>A
NG_008847.2:g.13762G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616242.5:c.-456G>A	ENSP00000482149.2:n.-456G>A
ENST00000682635.1:n.31G>A
ENST00000403799.8:c.-456G>A MANE Select	ENSP00000384247.3:n.-456G>A
ENST00000671824.1:c.-456G>A	ENSP00000500264.1:n.-456G>A
ENST00000673284.1:c.-456G>A	ENSP00000499852.1:n.-456G>A
ENST00000403799.7:c.-456G>A	ENSP00000384247.3:n.-456G>A
ENST00000476008.1:n.480+8282G>A
NM_000162.3:c.-456G>A	NP_000153.1:n.-456G>A
NM_000162.4:c.-456G>A	NP_000153.1:n.-456G>A
NM_001354800.1:c.-456G>A	NP_001341729.1:n.-456G>A
NM_000162.5:c.-456G>A MANE Select	NP_000153.1:n.-456G>A