Canonical Allele Identifier: CA1310070114

Gene: AGPS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177521284C= , CM000664.2:g.177521284C=	GRCh38
NC_000002.11:g.178386012C= , CM000664.1:g.178386012C=	GRCh37
NC_000002.10:g.178094258C=	NCBI36
NG_008968.1:g.133542C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.1713C= MANE Select	ENSP00000264167.4:p.Tyr571=
ENST00000637633.2:c.1713C=	ENSP00000490844.2:p.Tyr571=
ENST00000642466.2:c.1713C=	ENSP00000494433.2:p.Tyr571=
ENST00000679421.1:n.2942C=
ENST00000679459.1:c.1713C=	ENSP00000506137.1:p.Tyr571=
ENST00000679478.1:c.1443C=	ENSP00000506484.1:p.Tyr481=
ENST00000679994.1:c.1443C=	ENSP00000504957.1:p.Tyr481=
ENST00000680028.1:n.3077C=
ENST00000680155.1:c.1443C=	ENSP00000505333.1:p.Tyr481=
ENST00000680390.1:n.748C=
ENST00000680770.1:c.1713C=	ENSP00000505536.1:p.Tyr571=
ENST00000680893.1:c.*961C=	ENSP00000505929.1:n.*961C=
ENST00000681028.1:c.*140C=	ENSP00000506323.1:n.*140C=
ENST00000681032.1:c.*1091C=	ENSP00000505205.1:n.*1091C=
ENST00000681300.1:n.668C=
ENST00000681449.1:c.1443C=	ENSP00000505342.1:p.Tyr481=
ENST00000681565.1:c.*846C=	ENSP00000505620.1:n.*846C=
ENST00000681752.1:c.*1483C=	ENSP00000504994.1:n.*1483C=
ENST00000681891.1:n.5348C=
ENST00000264167.8:c.1713C=	ENSP00000264167.4:p.Tyr571=
ENST00000409888.1:c.351-45C=	ENSP00000386688.1:n.351-45C=
NM_003659.3:c.1713C=	NP_003650.1:p.Tyr571=
XM_011512041.1:c.1443C=	XP_011510343.1:p.Tyr481=
XM_011512042.1:c.1443C=	XP_011510344.1:p.Tyr481=
XM_011512043.1:c.978C=	XP_011510345.1:p.Tyr326=
XM_011512041.2:c.1443C=	XP_011510343.1:p.Tyr481=
XM_011512043.2:c.978C=	XP_011510345.1:p.Tyr326=
XR_001739007.2:n.1621C=
NM_003659.4:c.1713C= MANE Select	NP_003650.1:p.Tyr571=