Canonical Allele Identifier: CA2682574969

Gene: GCK

Linked Data

• gnomAD v4: 7-44189385-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189385C>A , CM000669.2:g.44189385C>A	GRCh38
NC_000007.13:g.44228984C>A , CM000669.1:g.44228984C>A	GRCh37
NC_000007.12:g.44195509C>A	NCBI36
NG_008847.1:g.5039G>T
NG_008847.2:g.13786G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-432G>T	ENSP00000482149.2:n.-432G>T
ENST00000682635.1:n.55G>T
ENST00000403799.8:c.-432G>T MANE Select	ENSP00000384247.3:n.-432G>T
ENST00000671824.1:c.-432G>T	ENSP00000500264.1:n.-432G>T
ENST00000673284.1:c.-432G>T	ENSP00000499852.1:n.-432G>T
ENST00000403799.7:c.-432G>T	ENSP00000384247.3:n.-432G>T
ENST00000476008.1:n.480+8306G>T
NM_000162.3:c.-432G>T	NP_000153.1:n.-432G>T
NM_000162.4:c.-432G>T	NP_000153.1:n.-432G>T
NM_001354800.1:c.-432G>T	NP_001341729.1:n.-432G>T
NM_000162.5:c.-432G>T MANE Select	NP_000153.1:n.-432G>T