Canonical Allele Identifier: CA367400103

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44186188A>T (hg19) ; chr7:g.44146589A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146589A>T , CM000669.2:g.44146589A>T	GRCh38
NC_000007.13:g.44186188A>T , CM000669.1:g.44186188A>T	GRCh37
NC_000007.12:g.44152713A>T	NCBI36
NG_008847.1:g.47835T>A
NG_008847.2:g.56582T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*891T>A	ENSP00000379142.4:n.*891T>A
ENST00000616242.5:c.*13T>A	ENSP00000482149.2:n.*13T>A
ENST00000683378.1:n.119T>A
ENST00000345378.7:c.896T>A	ENSP00000223366.2:p.Met299Lys
ENST00000403799.8:c.893T>A MANE Select	ENSP00000384247.3:p.Met298Lys
ENST00000671824.1:c.956T>A	ENSP00000500264.1:p.Met319Lys
ENST00000673284.1:c.893T>A	ENSP00000499852.1:p.Met298Lys
ENST00000345378.6:c.896T>A	ENSP00000223366.2:p.Met299Lys
ENST00000395796.7:c.890T>A	ENSP00000379142.3:p.Met297Lys
ENST00000403799.7:c.893T>A	ENSP00000384247.3:p.Met298Lys
ENST00000437084.1:c.842T>A	ENSP00000402840.1:p.Met281Lys
ENST00000473353.1:n.191T>A
ENST00000616242.4:c.890T>A	ENSP00000482149.1:p.Met297Lys
NM_000162.3:c.893T>A	NP_000153.1:p.Met298Lys
NM_033507.1:c.896T>A	NP_277042.1:p.Met299Lys
NM_033508.1:c.890T>A	NP_277043.1:p.Met297Lys
NM_000162.4:c.893T>A	NP_000153.1:p.Met298Lys
NM_001354800.1:c.893T>A	NP_001341729.1:p.Met298Lys
NM_001354801.1:c.8+30T>A	NP_001341730.1:n.8+30T>A
NM_033507.2:c.896T>A	NP_277042.1:p.Met299Lys
NM_033508.2:c.890T>A	NP_277043.1:p.Met297Lys
NM_000162.5:c.893T>A MANE Select	NP_000153.1:p.Met298Lys
NM_033507.3:c.896T>A	NP_277042.1:p.Met299Lys
NM_033508.3:c.890T>A	NP_277043.1:p.Met297Lys