Canonical Allele Identifier: CA367401774

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44189650T>G (hg19) ; chr7:g.44150051T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44150051T>G , CM000669.2:g.44150051T>G	GRCh38
NC_000007.13:g.44189650T>G , CM000669.1:g.44189650T>G	GRCh37
NC_000007.12:g.44156175T>G	NCBI36
NG_008847.1:g.44373A>C
NG_008847.2:g.53120A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*495A>C	ENSP00000379142.4:n.*495A>C
ENST00000616242.5:c.497A>C	ENSP00000482149.2:p.Asn166Thr
ENST00000682635.1:n.983A>C
ENST00000345378.7:c.500A>C	ENSP00000223366.2:p.Asn167Thr
ENST00000403799.8:c.497A>C MANE Select	ENSP00000384247.3:p.Asn166Thr
ENST00000671824.1:c.497A>C	ENSP00000500264.1:p.Asn166Thr
ENST00000673284.1:c.497A>C	ENSP00000499852.1:p.Asn166Thr
ENST00000345378.6:c.500A>C	ENSP00000223366.2:p.Asn167Thr
ENST00000395796.7:c.494A>C	ENSP00000379142.3:p.Asn165Thr
ENST00000403799.7:c.497A>C	ENSP00000384247.3:p.Asn166Thr
ENST00000437084.1:c.446A>C	ENSP00000402840.1:p.Asn149Thr
ENST00000616242.4:c.494A>C	ENSP00000482149.1:p.Asn165Thr
NM_000162.3:c.497A>C	NP_000153.1:p.Asn166Thr
NM_033507.1:c.500A>C	NP_277042.1:p.Asn167Thr
NM_033508.1:c.494A>C	NP_277043.1:p.Asn165Thr
NM_000162.4:c.497A>C	NP_000153.1:p.Asn166Thr
NM_001354800.1:c.497A>C	NP_001341729.1:p.Asn166Thr
NM_033507.2:c.500A>C	NP_277042.1:p.Asn167Thr
NM_033508.2:c.494A>C	NP_277043.1:p.Asn165Thr
NM_000162.5:c.497A>C MANE Select	NP_000153.1:p.Asn166Thr
NM_033507.3:c.500A>C	NP_277042.1:p.Asn167Thr
NM_033508.3:c.494A>C	NP_277043.1:p.Asn165Thr