Canonical Allele Identifier: CA1310058414

Gene: AGPS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177493170G= , CM000664.2:g.177493170G=	GRCh38
NC_000002.11:g.178357898G= , CM000664.1:g.178357898G=	GRCh37
NC_000002.10:g.178066144G=	NCBI36
NG_008968.1:g.105428G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003659.4:c.1256G= MANE Select	NP_003650.1:p.Arg419=
ENST00000264167.11:c.1256G= MANE Select	ENSP00000264167.4:p.Arg419=
NM_003659.3:c.1256G=	NP_003650.1:p.Arg419=
ENST00000264167.8:c.1256G=	ENSP00000264167.4:p.Arg419=
ENST00000409888.1:c.351-28159G=	ENSP00000386688.1:n.351-28159G=
ENST00000637633.2:c.1256G=	ENSP00000490844.2:p.Arg419=
ENST00000642466.2:c.1256G=	ENSP00000494433.2:p.Arg419=
ENST00000679421.1:n.2485G=
ENST00000679459.1:c.1256G=	ENSP00000506137.1:p.Arg419=
ENST00000679478.1:c.986G=	ENSP00000506484.1:p.Arg329=
ENST00000679994.1:c.986G=	ENSP00000504957.1:p.Arg329=
ENST00000680028.1:n.2620G=
ENST00000680155.1:c.986G=	ENSP00000505333.1:p.Arg329=
ENST00000680390.1:n.291G=
ENST00000680705.1:n.1300G=
ENST00000680770.1:c.1256G=	ENSP00000505536.1:p.Arg419=
ENST00000680893.1:c.*504G=	ENSP00000505929.1:n.*504G=
ENST00000680910.1:n.1286G=
ENST00000681028.1:c.986G=	ENSP00000506323.1:p.Arg329=
ENST00000681032.1:c.*634G=	ENSP00000505205.1:n.*634G=
ENST00000681300.1:n.211G=
ENST00000681449.1:c.986G=	ENSP00000505342.1:p.Arg329=
ENST00000681565.1:c.*389G=	ENSP00000505620.1:n.*389G=
ENST00000681752.1:c.*1026G=	ENSP00000504994.1:n.*1026G=
ENST00000681891.1:n.4891G=
XM_011512041.1:c.986G=	XP_011510343.1:p.Arg329=
XM_011512041.2:c.986G=	XP_011510343.1:p.Arg329=
XM_011512042.1:c.986G=	XP_011510344.1:p.Arg329=
XM_011512043.1:c.521G=	XP_011510345.1:p.Arg174=
XM_011512043.2:c.521G=	XP_011510345.1:p.Arg174=
XR_001739007.2:n.1164G=