Canonical Allele Identifier: CA1310058419
Gene: AGPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.177493182A= , CM000664.2:g.177493182A= GRCh38
NC_000002.11:g.178357910A= , CM000664.1:g.178357910A= GRCh37
NC_000002.10:g.178066156A= NCBI36
NG_008968.1:g.105440A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264167.11:c.1268A= MANE Select ENSP00000264167.4:p.Asn423=
ENST00000637633.2:c.1268A= ENSP00000490844.2:p.Asn423=
ENST00000642466.2:c.1268A= ENSP00000494433.2:p.Asn423=
ENST00000679421.1:n.2497A=
ENST00000679459.1:c.1268A= ENSP00000506137.1:p.Asn423=
ENST00000679478.1:c.998A= ENSP00000506484.1:p.Asn333=
ENST00000679994.1:c.998A= ENSP00000504957.1:p.Asn333=
ENST00000680028.1:n.2632A=
ENST00000680155.1:c.998A= ENSP00000505333.1:p.Asn333=
ENST00000680390.1:n.303A=
ENST00000680705.1:n.1312A=
ENST00000680770.1:c.1268A= ENSP00000505536.1:p.Asn423=
ENST00000680893.1:c.*516A= ENSP00000505929.1:n.*516A=
ENST00000680910.1:n.1298A=
ENST00000681028.1:c.998A= ENSP00000506323.1:p.Asn333=
ENST00000681032.1:c.*646A= ENSP00000505205.1:n.*646A=
ENST00000681300.1:n.223A=
ENST00000681449.1:c.998A= ENSP00000505342.1:p.Asn333=
ENST00000681565.1:c.*401A= ENSP00000505620.1:n.*401A=
ENST00000681752.1:c.*1038A= ENSP00000504994.1:n.*1038A=
ENST00000681891.1:n.4903A=
ENST00000264167.8:c.1268A= ENSP00000264167.4:p.Asn423=
ENST00000409888.1:c.351-28147A= ENSP00000386688.1:n.351-28147A=
NM_003659.3:c.1268A= NP_003650.1:p.Asn423=
XM_011512041.1:c.998A= XP_011510343.1:p.Asn333=
XM_011512042.1:c.998A= XP_011510344.1:p.Asn333=
XM_011512043.1:c.533A= XP_011510345.1:p.Asn178=
XM_011512041.2:c.998A= XP_011510343.1:p.Asn333=
XM_011512043.2:c.533A= XP_011510345.1:p.Asn178=
XR_001739007.2:n.1176A=
NM_003659.4:c.1268A= MANE Select NP_003650.1:p.Asn423=