Canonical Allele Identifier: CA1703653848

Gene: GCK

Linked Data

• dbSNP Id: rs2096324964

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44189414T>C , CM000669.2:g.44189414T>C	GRCh38
NC_000007.13:g.44229013T>C , CM000669.1:g.44229013T>C	GRCh37
NC_000007.12:g.44195538T>C	NCBI36
NG_008847.1:g.5010A>G
NG_008847.2:g.13757A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616242.5:c.-461A>G	ENSP00000482149.2:n.-461A>G
ENST00000682635.1:n.26A>G
ENST00000403799.8:c.-461A>G MANE Select	ENSP00000384247.3:n.-461A>G
ENST00000671824.1:c.-461A>G	ENSP00000500264.1:n.-461A>G
ENST00000673284.1:c.-461A>G	ENSP00000499852.1:n.-461A>G
ENST00000403799.7:c.-461A>G	ENSP00000384247.3:n.-461A>G
ENST00000476008.1:n.480+8277A>G
NM_000162.3:c.-461A>G	NP_000153.1:n.-461A>G
NM_000162.4:c.-461A>G	NP_000153.1:n.-461A>G
NM_001354800.1:c.-461A>G	NP_001341729.1:n.-461A>G
NM_000162.5:c.-461A>G MANE Select	NP_000153.1:n.-461A>G