Canonical Allele Identifier: CA838795249

Gene: GCK

Linked Data

• dbSNP Id: rs1465280847
• gnomAD v3: 7-44189394-G-A
• gnomAD v4: 7-44189394-G-A
• MyVariant Identifiers: chr7:g.44228993G>A (hg19) ; chr7:g.44189394G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189394G>A , CM000669.2:g.44189394G>A	GRCh38
NC_000007.13:g.44228993G>A , CM000669.1:g.44228993G>A	GRCh37
NC_000007.12:g.44195518G>A	NCBI36
NG_008847.1:g.5030C>T
NG_008847.2:g.13777C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-441C>T	ENSP00000482149.2:n.-441C>T
ENST00000682635.1:n.46C>T
ENST00000403799.8:c.-441C>T MANE Select	ENSP00000384247.3:n.-441C>T
ENST00000671824.1:c.-441C>T	ENSP00000500264.1:n.-441C>T
ENST00000673284.1:c.-441C>T	ENSP00000499852.1:n.-441C>T
ENST00000403799.7:c.-441C>T	ENSP00000384247.3:n.-441C>T
ENST00000476008.1:n.480+8297C>T
NM_000162.3:c.-441C>T	NP_000153.1:n.-441C>T
NM_000162.4:c.-441C>T	NP_000153.1:n.-441C>T
NM_001354800.1:c.-441C>T	NP_001341729.1:n.-441C>T
NM_000162.5:c.-441C>T MANE Select	NP_000153.1:n.-441C>T