Canonical Allele Identifier: CA367400564

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44187327T>G (hg19) ; chr7:g.44147728T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147728T>G , CM000669.2:g.44147728T>G	GRCh38
NC_000007.13:g.44187327T>G , CM000669.1:g.44187327T>G	GRCh37
NC_000007.12:g.44153852T>G	NCBI36
NG_008847.1:g.46696A>C
NG_008847.2:g.55443A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*783A>C	ENSP00000379142.4:n.*783A>C
ENST00000616242.5:c.785A>C	ENSP00000482149.2:p.Asp262Ala
ENST00000345378.7:c.788A>C	ENSP00000223366.2:p.Asp263Ala
ENST00000403799.8:c.785A>C MANE Select	ENSP00000384247.3:p.Asp262Ala
ENST00000671824.1:c.785A>C	ENSP00000500264.1:p.Asp262Ala
ENST00000673284.1:c.785A>C	ENSP00000499852.1:p.Asp262Ala
ENST00000345378.6:c.788A>C	ENSP00000223366.2:p.Asp263Ala
ENST00000395796.7:c.782A>C	ENSP00000379142.3:p.Asp261Ala
ENST00000403799.7:c.785A>C	ENSP00000384247.3:p.Asp262Ala
ENST00000437084.1:c.734A>C	ENSP00000402840.1:p.Asp245Ala
ENST00000616242.4:c.782A>C	ENSP00000482149.1:p.Asp261Ala
NM_000162.3:c.785A>C	NP_000153.1:p.Asp262Ala
NM_033507.1:c.788A>C	NP_277042.1:p.Asp263Ala
NM_033508.1:c.782A>C	NP_277043.1:p.Asp261Ala
XR_927223.1:n.62T>G
NM_000162.4:c.785A>C	NP_000153.1:p.Asp262Ala
NM_001354800.1:c.785A>C	NP_001341729.1:p.Asp262Ala
NM_033507.2:c.788A>C	NP_277042.1:p.Asp263Ala
NM_033508.2:c.782A>C	NP_277043.1:p.Asp261Ala
XR_927223.2:n.62T>G
NM_000162.5:c.785A>C MANE Select	NP_000153.1:p.Asp262Ala
NM_033507.3:c.788A>C	NP_277042.1:p.Asp263Ala
NM_033508.3:c.782A>C	NP_277043.1:p.Asp261Ala