Canonical Allele Identifier: CA838795246

Gene: GCK

Linked Data

• dbSNP Id: rs1172349196
• gnomAD v3: 7-44189393-G-C
• gnomAD v4: 7-44189393-G-C
• MyVariant Identifiers: chr7:g.44228992G>C (hg19) ; chr7:g.44189393G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189393G>C , CM000669.2:g.44189393G>C	GRCh38
NC_000007.13:g.44228992G>C , CM000669.1:g.44228992G>C	GRCh37
NC_000007.12:g.44195517G>C	NCBI36
NG_008847.1:g.5031C>G
NG_008847.2:g.13778C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-440C>G	ENSP00000482149.2:n.-440C>G
ENST00000682635.1:n.47C>G
ENST00000403799.8:c.-440C>G MANE Select	ENSP00000384247.3:n.-440C>G
ENST00000671824.1:c.-440C>G	ENSP00000500264.1:n.-440C>G
ENST00000673284.1:c.-440C>G	ENSP00000499852.1:n.-440C>G
ENST00000403799.7:c.-440C>G	ENSP00000384247.3:n.-440C>G
ENST00000476008.1:n.480+8298C>G
NM_000162.3:c.-440C>G	NP_000153.1:n.-440C>G
NM_000162.4:c.-440C>G	NP_000153.1:n.-440C>G
NM_001354800.1:c.-440C>G	NP_001341729.1:n.-440C>G
NM_000162.5:c.-440C>G MANE Select	NP_000153.1:n.-440C>G