Canonical Allele Identifier: CA367398338

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44185126A>G (hg19) ; chr7:g.44145527A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145527A>G , CM000669.2:g.44145527A>G	GRCh38
NC_000007.13:g.44185126A>G , CM000669.1:g.44185126A>G	GRCh37
NC_000007.12:g.44151651A>G	NCBI36
NG_008847.1:g.48897T>C
NG_008847.2:g.57644T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1221T>C	ENSP00000379142.4:n.*1221T>C
ENST00000616242.5:c.*343T>C	ENSP00000482149.2:n.*343T>C
ENST00000683378.1:n.449T>C
ENST00000336642.9:c.257T>C	ENSP00000338009.5:p.Val86Ala
ENST00000345378.7:c.1226T>C	ENSP00000223366.2:p.Val409Ala
ENST00000403799.8:c.1223T>C MANE Select	ENSP00000384247.3:p.Val408Ala
ENST00000671824.1:c.1286T>C	ENSP00000500264.1:p.Val429Ala
ENST00000672743.1:n.235T>C
ENST00000673284.1:c.1223T>C	ENSP00000499852.1:p.Val408Ala
ENST00000336642.8:c.275T>C	ENSP00000338009.4:p.Val92Ala
ENST00000345378.6:c.1226T>C	ENSP00000223366.2:p.Val409Ala
ENST00000395796.7:c.1220T>C	ENSP00000379142.3:p.Val407Ala
ENST00000403799.7:c.1223T>C	ENSP00000384247.3:p.Val408Ala
ENST00000437084.1:c.1172T>C	ENSP00000402840.1:p.Val391Ala
ENST00000459642.1:n.603T>C
ENST00000616242.4:c.1220T>C	ENSP00000482149.1:p.Val407Ala
NM_000162.3:c.1223T>C	NP_000153.1:p.Val408Ala
NM_033507.1:c.1226T>C	NP_277042.1:p.Val409Ala
NM_033508.1:c.1220T>C	NP_277043.1:p.Val407Ala
NM_000162.4:c.1223T>C	NP_000153.1:p.Val408Ala
NM_001354800.1:c.1223T>C	NP_001341729.1:p.Val408Ala
NM_001354801.1:c.212T>C	NP_001341730.1:p.Val71Ala
NM_001354802.1:c.83T>C	NP_001341731.1:p.Val28Ala
NM_001354803.1:c.257T>C	NP_001341732.1:p.Val86Ala
NM_033507.2:c.1226T>C	NP_277042.1:p.Val409Ala
NM_033508.2:c.1220T>C	NP_277043.1:p.Val407Ala
XM_024446707.1:c.83T>C	XP_024302475.1:p.Val28Ala
NM_000162.5:c.1223T>C MANE Select	NP_000153.1:p.Val408Ala
NM_033507.3:c.1226T>C	NP_277042.1:p.Val409Ala
NM_033508.3:c.1220T>C	NP_277043.1:p.Val407Ala
NM_001354803.2:c.257T>C	NP_001341732.1:p.Val86Ala