Canonical Allele Identifier: CA573791484

Gene: GCK

Linked Data

• dbSNP Id: rs1176039605
• gnomAD v2: 7-44228987-C-A
• gnomAD v3: 7-44189388-C-A
• gnomAD v4: 7-44189388-C-A
• MyVariant Identifiers: chr7:g.44228987C>A (hg19) ; chr7:g.44189388C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189388C>A , CM000669.2:g.44189388C>A	GRCh38
NC_000007.13:g.44228987C>A , CM000669.1:g.44228987C>A	GRCh37
NC_000007.12:g.44195512C>A	NCBI36
NG_008847.1:g.5036G>T
NG_008847.2:g.13783G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-435G>T	ENSP00000482149.2:n.-435G>T
ENST00000682635.1:n.52G>T
ENST00000403799.8:c.-435G>T MANE Select	ENSP00000384247.3:n.-435G>T
ENST00000671824.1:c.-435G>T	ENSP00000500264.1:n.-435G>T
ENST00000673284.1:c.-435G>T	ENSP00000499852.1:n.-435G>T
ENST00000403799.7:c.-435G>T	ENSP00000384247.3:n.-435G>T
ENST00000476008.1:n.480+8303G>T
NM_000162.3:c.-435G>T	NP_000153.1:n.-435G>T
NM_000162.4:c.-435G>T	NP_000153.1:n.-435G>T
NM_001354800.1:c.-435G>T	NP_001341729.1:n.-435G>T
NM_000162.5:c.-435G>T MANE Select	NP_000153.1:n.-435G>T