Canonical Allele Identifier: CA1703651356

Gene: GCK

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44184122G>C , CM000669.2:g.44184122G>C	GRCh38
NC_000007.13:g.44223721G>C , CM000669.1:g.44223721G>C	GRCh37
NC_000007.12:g.44190246G>C	NCBI36
NG_008847.1:g.10302C>G
NG_008847.2:g.19049C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616242.5:c.45+4787C>G	ENSP00000482149.2:n.45+4787C>G
ENST00000682635.1:n.531+4787C>G
ENST00000403799.8:c.45+4787C>G MANE Select	ENSP00000384247.3:n.45+4787C>G
ENST00000671824.1:c.45+4787C>G	ENSP00000500264.1:n.45+4787C>G
ENST00000673284.1:c.45+4787C>G	ENSP00000499852.1:n.45+4787C>G
ENST00000403799.7:c.45+4787C>G	ENSP00000384247.3:n.45+4787C>G
ENST00000437084.1:c.45+4787C>G	ENSP00000402840.1:n.45+4787C>G
ENST00000476008.1:n.480+13569C>G
NM_000162.3:c.45+4787C>G	NP_000153.1:n.45+4787C>G
XR_927221.1:n.379G>C
XR_927222.1:n.1702G>C
NM_000162.4:c.45+4787C>G	NP_000153.1:n.45+4787C>G
NM_001354800.1:c.45+4787C>G	NP_001341729.1:n.45+4787C>G
XR_927221.2:n.379G>C
XR_927222.2:n.1702G>C
NM_000162.5:c.45+4787C>G MANE Select	NP_000153.1:n.45+4787C>G