Canonical Allele Identifier: CA1310044914
Gene: AGPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.177461976A= , CM000664.2:g.177461976A= GRCh38
NC_000002.11:g.178326704A= , CM000664.1:g.178326704A= GRCh37
NC_000002.10:g.178034950A= NCBI36
NG_008968.1:g.74234A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264167.11:c.954A= MANE Select ENSP00000264167.4:p.Ala318=
ENST00000460342.2:n.2366A=
ENST00000637633.2:c.954A= ENSP00000490844.2:p.Ala318=
ENST00000642466.2:c.954A= ENSP00000494433.2:p.Ala318=
ENST00000679421.1:n.2183A=
ENST00000679459.1:c.954A= ENSP00000506137.1:p.Ala318=
ENST00000679478.1:c.684A= ENSP00000506484.1:p.Ala228=
ENST00000679639.1:n.757A=
ENST00000679994.1:c.684A= ENSP00000504957.1:p.Ala228=
ENST00000680028.1:n.2318A=
ENST00000680155.1:c.684A= ENSP00000505333.1:p.Ala228=
ENST00000680705.1:n.998A=
ENST00000680770.1:c.954A= ENSP00000505536.1:p.Ala318=
ENST00000680893.1:c.*202A= ENSP00000505929.1:n.*202A=
ENST00000680910.1:n.984A=
ENST00000681028.1:c.684A= ENSP00000506323.1:p.Ala228=
ENST00000681032.1:c.*332A= ENSP00000505205.1:n.*332A=
ENST00000681449.1:c.684A= ENSP00000505342.1:p.Ala228=
ENST00000681565.1:c.954A= ENSP00000505620.1:p.Ala318=
ENST00000681752.1:c.*724A= ENSP00000504994.1:n.*724A=
ENST00000681891.1:n.4698A=
ENST00000264167.8:c.954A= ENSP00000264167.4:p.Ala318=
ENST00000409888.1:c.350+41618A= ENSP00000386688.1:n.350+41618A=
NM_003659.3:c.954A= NP_003650.1:p.Ala318=
XM_011512041.1:c.684A= XP_011510343.1:p.Ala228=
XM_011512042.1:c.684A= XP_011510344.1:p.Ala228=
XM_011512043.1:c.219A= XP_011510345.1:p.Ala73=
XM_011512044.1:c.954A= XP_011510346.1:p.Ala318=
XM_011512045.1:c.954A= XP_011510347.1:p.Ala318=
XM_011512041.2:c.684A= XP_011510343.1:p.Ala228=
XM_011512043.2:c.219A= XP_011510345.1:p.Ala73=
XR_001739007.2:n.971A=
NM_003659.4:c.954A= MANE Select NP_003650.1:p.Ala318=