Canonical Allele Identifier: CA1310070119

Gene: AGPS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177521295C= , CM000664.2:g.177521295C=	GRCh38
NC_000002.11:g.178386023C= , CM000664.1:g.178386023C=	GRCh37
NC_000002.10:g.178094269C=	NCBI36
NG_008968.1:g.133553C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.1724C= MANE Select	ENSP00000264167.4:p.Ala575=
ENST00000637633.2:c.1724C=	ENSP00000490844.2:p.Ala575=
ENST00000642466.2:c.1724C=	ENSP00000494433.2:p.Ala575=
ENST00000679421.1:n.2953C=
ENST00000679459.1:c.1724C=	ENSP00000506137.1:p.Ala575=
ENST00000679478.1:c.1454C=	ENSP00000506484.1:p.Ala485=
ENST00000679994.1:c.1454C=	ENSP00000504957.1:p.Ala485=
ENST00000680028.1:n.3088C=
ENST00000680155.1:c.1454C=	ENSP00000505333.1:p.Ala485=
ENST00000680390.1:n.759C=
ENST00000680770.1:c.1724C=	ENSP00000505536.1:p.Ala575=
ENST00000680893.1:c.*972C=	ENSP00000505929.1:n.*972C=
ENST00000681028.1:c.*151C=	ENSP00000506323.1:n.*151C=
ENST00000681032.1:c.*1102C=	ENSP00000505205.1:n.*1102C=
ENST00000681300.1:n.679C=
ENST00000681449.1:c.1454C=	ENSP00000505342.1:p.Ala485=
ENST00000681565.1:c.*857C=	ENSP00000505620.1:n.*857C=
ENST00000681752.1:c.*1494C=	ENSP00000504994.1:n.*1494C=
ENST00000681891.1:n.5359C=
ENST00000264167.8:c.1724C=	ENSP00000264167.4:p.Ala575=
ENST00000409888.1:c.351-34C=	ENSP00000386688.1:n.351-34C=
NM_003659.3:c.1724C=	NP_003650.1:p.Ala575=
XM_011512041.1:c.1454C=	XP_011510343.1:p.Ala485=
XM_011512042.1:c.1454C=	XP_011510344.1:p.Ala485=
XM_011512043.1:c.989C=	XP_011510345.1:p.Ala330=
XM_011512041.2:c.1454C=	XP_011510343.1:p.Ala485=
XM_011512043.2:c.989C=	XP_011510345.1:p.Ala330=
XR_001739007.2:n.1632C=
NM_003659.4:c.1724C= MANE Select	NP_003650.1:p.Ala575=