Canonical Allele Identifier: CA349704407

Gene: AGPS

Linked Data

• MyVariant Identifiers: chr2:g.178326681G>A (hg19) ; chr2:g.177461953G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177461953G>A , CM000664.2:g.177461953G>A	GRCh38
NC_000002.11:g.178326681G>A , CM000664.1:g.178326681G>A	GRCh37
NC_000002.10:g.178034927G>A	NCBI36
NG_008968.1:g.74211G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264167.11:c.931G>A MANE Select	ENSP00000264167.4:p.Gly311Arg
ENST00000460342.2:n.2343G>A
ENST00000637633.2:c.931G>A	ENSP00000490844.2:p.Gly311Arg
ENST00000642466.2:c.931G>A	ENSP00000494433.2:p.Gly311Arg
ENST00000679421.1:n.2160G>A
ENST00000679459.1:c.931G>A	ENSP00000506137.1:p.Gly311Arg
ENST00000679478.1:c.661G>A	ENSP00000506484.1:p.Gly221Arg
ENST00000679639.1:n.734G>A
ENST00000679994.1:c.661G>A	ENSP00000504957.1:p.Gly221Arg
ENST00000680028.1:n.2295G>A
ENST00000680155.1:c.661G>A	ENSP00000505333.1:p.Gly221Arg
ENST00000680705.1:n.975G>A
ENST00000680770.1:c.931G>A	ENSP00000505536.1:p.Gly311Arg
ENST00000680893.1:c.*179G>A	ENSP00000505929.1:n.*179G>A
ENST00000680910.1:n.961G>A
ENST00000681028.1:c.661G>A	ENSP00000506323.1:p.Gly221Arg
ENST00000681032.1:c.*309G>A	ENSP00000505205.1:n.*309G>A
ENST00000681449.1:c.661G>A	ENSP00000505342.1:p.Gly221Arg
ENST00000681565.1:c.931G>A	ENSP00000505620.1:p.Gly311Arg
ENST00000681752.1:c.*701G>A	ENSP00000504994.1:n.*701G>A
ENST00000681891.1:n.4675G>A
ENST00000264167.8:c.931G>A	ENSP00000264167.4:p.Gly311Arg
ENST00000409888.1:c.350+41595G>A	ENSP00000386688.1:n.350+41595G>A
NM_003659.3:c.931G>A	NP_003650.1:p.Gly311Arg
XM_011512041.1:c.661G>A	XP_011510343.1:p.Gly221Arg
XM_011512042.1:c.661G>A	XP_011510344.1:p.Gly221Arg
XM_011512043.1:c.196G>A	XP_011510345.1:p.Gly66Arg
XM_011512044.1:c.931G>A	XP_011510346.1:p.Gly311Arg
XM_011512045.1:c.931G>A	XP_011510347.1:p.Gly311Arg
XM_011512041.2:c.661G>A	XP_011510343.1:p.Gly221Arg
XM_011512043.2:c.196G>A	XP_011510345.1:p.Gly66Arg
XR_001739007.2:n.948G>A
NM_003659.4:c.931G>A MANE Select	NP_003650.1:p.Gly311Arg