Canonical Allele Identifier: CA2682574924

Gene: GCK

Linked Data

• gnomAD v4: 7-44189370-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189370T>C , CM000669.2:g.44189370T>C	GRCh38
NC_000007.13:g.44228969T>C , CM000669.1:g.44228969T>C	GRCh37
NC_000007.12:g.44195494T>C	NCBI36
NG_008847.1:g.5054A>G
NG_008847.2:g.13801A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000616242.5:c.-417A>G	ENSP00000482149.2:n.-417A>G
ENST00000682635.1:n.70A>G
ENST00000403799.8:c.-417A>G MANE Select	ENSP00000384247.3:n.-417A>G
ENST00000671824.1:c.-417A>G	ENSP00000500264.1:n.-417A>G
ENST00000673284.1:c.-417A>G	ENSP00000499852.1:n.-417A>G
ENST00000403799.7:c.-417A>G	ENSP00000384247.3:n.-417A>G
ENST00000476008.1:n.480+8321A>G
NM_000162.3:c.-417A>G	NP_000153.1:n.-417A>G
NM_000162.4:c.-417A>G	NP_000153.1:n.-417A>G
NM_001354800.1:c.-417A>G	NP_001341729.1:n.-417A>G
NM_000162.5:c.-417A>G MANE Select	NP_000153.1:n.-417A>G