Canonical Allele Identifier: CA1310070120

Gene: AGPS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177521300A= , CM000664.2:g.177521300A=	GRCh38
NC_000002.11:g.178386028A= , CM000664.1:g.178386028A=	GRCh37
NC_000002.10:g.178094274A=	NCBI36
NG_008968.1:g.133558A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.1729A= MANE Select	ENSP00000264167.4:p.Ile577=
ENST00000637633.2:c.1729A=	ENSP00000490844.2:p.Ile577=
ENST00000642466.2:c.1729A=	ENSP00000494433.2:p.Ile577=
ENST00000679421.1:n.2958A=
ENST00000679459.1:c.1729A=	ENSP00000506137.1:p.Ile577=
ENST00000679478.1:c.1459A=	ENSP00000506484.1:p.Ile487=
ENST00000679994.1:c.1459A=	ENSP00000504957.1:p.Ile487=
ENST00000680028.1:n.3093A=
ENST00000680155.1:c.1459A=	ENSP00000505333.1:p.Ile487=
ENST00000680390.1:n.764A=
ENST00000680770.1:c.1729A=	ENSP00000505536.1:p.Ile577=
ENST00000680893.1:c.*977A=	ENSP00000505929.1:n.*977A=
ENST00000681028.1:c.*156A=	ENSP00000506323.1:n.*156A=
ENST00000681032.1:c.*1107A=	ENSP00000505205.1:n.*1107A=
ENST00000681300.1:n.684A=
ENST00000681449.1:c.1459A=	ENSP00000505342.1:p.Ile487=
ENST00000681565.1:c.*862A=	ENSP00000505620.1:n.*862A=
ENST00000681752.1:c.*1499A=	ENSP00000504994.1:n.*1499A=
ENST00000681891.1:n.5364A=
ENST00000264167.8:c.1729A=	ENSP00000264167.4:p.Ile577=
ENST00000409888.1:c.351-29A=	ENSP00000386688.1:n.351-29A=
NM_003659.3:c.1729A=	NP_003650.1:p.Ile577=
XM_011512041.1:c.1459A=	XP_011510343.1:p.Ile487=
XM_011512042.1:c.1459A=	XP_011510344.1:p.Ile487=
XM_011512043.1:c.994A=	XP_011510345.1:p.Ile332=
XM_011512041.2:c.1459A=	XP_011510343.1:p.Ile487=
XM_011512043.2:c.994A=	XP_011510345.1:p.Ile332=
XR_001739007.2:n.1637A=
NM_003659.4:c.1729A= MANE Select	NP_003650.1:p.Ile577=