Canonical Allele Identifier: CA2530936521

Gene: GCK

Linked Data

• gnomAD v4: 7-44153565-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153565G>C , CM000669.2:g.44153565G>C	GRCh38
NC_000007.13:g.44193164G>C , CM000669.1:g.44193164G>C	GRCh37
NC_000007.12:g.44159689G>C	NCBI36
NG_008847.1:g.40859C>G
NG_008847.2:g.49606C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*44-102C>G	ENSP00000379142.4:n.*44-102C>G
ENST00000616242.5:c.46-102C>G	ENSP00000482149.2:n.46-102C>G
ENST00000682635.1:n.532-102C>G
ENST00000345378.7:c.49-102C>G	ENSP00000223366.2:n.49-102C>G
ENST00000403799.8:c.46-102C>G MANE Select	ENSP00000384247.3:n.46-102C>G
ENST00000671824.1:c.46-102C>G	ENSP00000500264.1:n.46-102C>G
ENST00000673284.1:c.46-102C>G	ENSP00000499852.1:n.46-102C>G
ENST00000345378.6:c.49-102C>G	ENSP00000223366.2:n.49-102C>G
ENST00000395796.7:c.43-102C>G	ENSP00000379142.3:n.43-102C>G
ENST00000403799.7:c.46-102C>G	ENSP00000384247.3:n.46-102C>G
ENST00000437084.1:c.46-102C>G	ENSP00000402840.1:n.46-102C>G
ENST00000476008.1:n.481-102C>G
ENST00000616242.4:c.43-102C>G	ENSP00000482149.1:n.43-102C>G
NM_000162.3:c.46-102C>G	NP_000153.1:n.46-102C>G
NM_033507.1:c.49-102C>G	NP_277042.1:n.49-102C>G
NM_033508.1:c.43-102C>G	NP_277043.1:n.43-102C>G
NM_000162.4:c.46-102C>G	NP_000153.1:n.46-102C>G
NM_001354800.1:c.46-102C>G	NP_001341729.1:n.46-102C>G
NM_033507.2:c.49-102C>G	NP_277042.1:n.49-102C>G
NM_033508.2:c.43-102C>G	NP_277043.1:n.43-102C>G
NM_000162.5:c.46-102C>G MANE Select	NP_000153.1:n.46-102C>G
NM_033507.3:c.49-102C>G	NP_277042.1:n.49-102C>G
NM_033508.3:c.43-102C>G	NP_277043.1:n.43-102C>G