Canonical Allele Identifier: CA1310044920

Gene: AGPS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177462009C= , CM000664.2:g.177462009C=	GRCh38
NC_000002.11:g.178326737C= , CM000664.1:g.178326737C=	GRCh37
NC_000002.10:g.178034983C=	NCBI36
NG_008968.1:g.74267C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.987C= MANE Select	ENSP00000264167.4:p.Ile329=
ENST00000460342.2:n.2399C=
ENST00000637633.2:c.987C=	ENSP00000490844.2:p.Ile329=
ENST00000642466.2:c.987C=	ENSP00000494433.2:p.Ile329=
ENST00000679421.1:n.2216C=
ENST00000679459.1:c.987C=	ENSP00000506137.1:p.Ile329=
ENST00000679478.1:c.717C=	ENSP00000506484.1:p.Ile239=
ENST00000679639.1:n.790C=
ENST00000679994.1:c.717C=	ENSP00000504957.1:p.Ile239=
ENST00000680028.1:n.2351C=
ENST00000680155.1:c.717C=	ENSP00000505333.1:p.Ile239=
ENST00000680705.1:n.1031C=
ENST00000680770.1:c.987C=	ENSP00000505536.1:p.Ile329=
ENST00000680893.1:c.*235C=	ENSP00000505929.1:n.*235C=
ENST00000680910.1:n.1017C=
ENST00000681028.1:c.717C=	ENSP00000506323.1:p.Ile239=
ENST00000681032.1:c.*365C=	ENSP00000505205.1:n.*365C=
ENST00000681449.1:c.717C=	ENSP00000505342.1:p.Ile239=
ENST00000681565.1:c.987C=	ENSP00000505620.1:p.Ile329=
ENST00000681752.1:c.*757C=	ENSP00000504994.1:n.*757C=
ENST00000681891.1:n.4731C=
ENST00000264167.8:c.987C=	ENSP00000264167.4:p.Ile329=
ENST00000409888.1:c.350+41651C=	ENSP00000386688.1:n.350+41651C=
NM_003659.3:c.987C=	NP_003650.1:p.Ile329=
XM_011512041.1:c.717C=	XP_011510343.1:p.Ile239=
XM_011512042.1:c.717C=	XP_011510344.1:p.Ile239=
XM_011512043.1:c.252C=	XP_011510345.1:p.Ile84=
XM_011512044.1:c.987C=	XP_011510346.1:p.Ile329=
XM_011512045.1:c.987C=	XP_011510347.1:p.Ile329=
XM_011512041.2:c.717C=	XP_011510343.1:p.Ile239=
XM_011512043.2:c.252C=	XP_011510345.1:p.Ile84=
XR_001739007.2:n.1004C=
NM_003659.4:c.987C= MANE Select	NP_003650.1:p.Ile329=