Canonical Allele Identifier: CA349704417

Gene: AGPS

Linked Data

• MyVariant Identifiers: chr2:g.178326685G>C (hg19) ; chr2:g.177461957G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177461957G>C , CM000664.2:g.177461957G>C	GRCh38
NC_000002.11:g.178326685G>C , CM000664.1:g.178326685G>C	GRCh37
NC_000002.10:g.178034931G>C	NCBI36
NG_008968.1:g.74215G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264167.11:c.935G>C MANE Select	ENSP00000264167.4:p.Gly312Ala
ENST00000460342.2:n.2347G>C
ENST00000637633.2:c.935G>C	ENSP00000490844.2:p.Gly312Ala
ENST00000642466.2:c.935G>C	ENSP00000494433.2:p.Gly312Ala
ENST00000679421.1:n.2164G>C
ENST00000679459.1:c.935G>C	ENSP00000506137.1:p.Gly312Ala
ENST00000679478.1:c.665G>C	ENSP00000506484.1:p.Gly222Ala
ENST00000679639.1:n.738G>C
ENST00000679994.1:c.665G>C	ENSP00000504957.1:p.Gly222Ala
ENST00000680028.1:n.2299G>C
ENST00000680155.1:c.665G>C	ENSP00000505333.1:p.Gly222Ala
ENST00000680705.1:n.979G>C
ENST00000680770.1:c.935G>C	ENSP00000505536.1:p.Gly312Ala
ENST00000680893.1:c.*183G>C	ENSP00000505929.1:n.*183G>C
ENST00000680910.1:n.965G>C
ENST00000681028.1:c.665G>C	ENSP00000506323.1:p.Gly222Ala
ENST00000681032.1:c.*313G>C	ENSP00000505205.1:n.*313G>C
ENST00000681449.1:c.665G>C	ENSP00000505342.1:p.Gly222Ala
ENST00000681565.1:c.935G>C	ENSP00000505620.1:p.Gly312Ala
ENST00000681752.1:c.*705G>C	ENSP00000504994.1:n.*705G>C
ENST00000681891.1:n.4679G>C
ENST00000264167.8:c.935G>C	ENSP00000264167.4:p.Gly312Ala
ENST00000409888.1:c.350+41599G>C	ENSP00000386688.1:n.350+41599G>C
NM_003659.3:c.935G>C	NP_003650.1:p.Gly312Ala
XM_011512041.1:c.665G>C	XP_011510343.1:p.Gly222Ala
XM_011512042.1:c.665G>C	XP_011510344.1:p.Gly222Ala
XM_011512043.1:c.200G>C	XP_011510345.1:p.Gly67Ala
XM_011512044.1:c.935G>C	XP_011510346.1:p.Gly312Ala
XM_011512045.1:c.935G>C	XP_011510347.1:p.Gly312Ala
XM_011512041.2:c.665G>C	XP_011510343.1:p.Gly222Ala
XM_011512043.2:c.200G>C	XP_011510345.1:p.Gly67Ala
XR_001739007.2:n.952G>C
NM_003659.4:c.935G>C MANE Select	NP_003650.1:p.Gly312Ala