Canonical Allele Identifier: CA1310070116

Gene: AGPS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.177521288G= , CM000664.2:g.177521288G=	GRCh38
NC_000002.11:g.178386016G= , CM000664.1:g.178386016G=	GRCh37
NC_000002.10:g.178094262G=	NCBI36
NG_008968.1:g.133546G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264167.11:c.1717G= MANE Select	ENSP00000264167.4:p.Ala573=
ENST00000637633.2:c.1717G=	ENSP00000490844.2:p.Ala573=
ENST00000642466.2:c.1717G=	ENSP00000494433.2:p.Ala573=
ENST00000679421.1:n.2946G=
ENST00000679459.1:c.1717G=	ENSP00000506137.1:p.Ala573=
ENST00000679478.1:c.1447G=	ENSP00000506484.1:p.Ala483=
ENST00000679994.1:c.1447G=	ENSP00000504957.1:p.Ala483=
ENST00000680028.1:n.3081G=
ENST00000680155.1:c.1447G=	ENSP00000505333.1:p.Ala483=
ENST00000680390.1:n.752G=
ENST00000680770.1:c.1717G=	ENSP00000505536.1:p.Ala573=
ENST00000680893.1:c.*965G=	ENSP00000505929.1:n.*965G=
ENST00000681028.1:c.*144G=	ENSP00000506323.1:n.*144G=
ENST00000681032.1:c.*1095G=	ENSP00000505205.1:n.*1095G=
ENST00000681300.1:n.672G=
ENST00000681449.1:c.1447G=	ENSP00000505342.1:p.Ala483=
ENST00000681565.1:c.*850G=	ENSP00000505620.1:n.*850G=
ENST00000681752.1:c.*1487G=	ENSP00000504994.1:n.*1487G=
ENST00000681891.1:n.5352G=
ENST00000264167.8:c.1717G=	ENSP00000264167.4:p.Ala573=
ENST00000409888.1:c.351-41G=	ENSP00000386688.1:n.351-41G=
NM_003659.3:c.1717G=	NP_003650.1:p.Ala573=
XM_011512041.1:c.1447G=	XP_011510343.1:p.Ala483=
XM_011512042.1:c.1447G=	XP_011510344.1:p.Ala483=
XM_011512043.1:c.982G=	XP_011510345.1:p.Ala328=
XM_011512041.2:c.1447G=	XP_011510343.1:p.Ala483=
XM_011512043.2:c.982G=	XP_011510345.1:p.Ala328=
XR_001739007.2:n.1625G=
NM_003659.4:c.1717G= MANE Select	NP_003650.1:p.Ala573=