Canonical Allele Identifier: CA2753310270
Gene: AGPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.177462007dup , CM000664.2:g.177462007dup GRCh38
NC_000002.11:g.178326735dup , CM000664.1:g.178326735dup GRCh37
NC_000002.10:g.178034981dup NCBI36
NG_008968.1:g.74265dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264167.11:c.985dup MANE Select ENSP00000264167.4:p.Ile329AsnfsTer14
ENST00000460342.2:n.2397dup
ENST00000637633.2:c.985dup ENSP00000490844.2:p.Ile329AsnfsTer14
ENST00000642466.2:c.985dup ENSP00000494433.2:p.Ile329AsnfsTer14
ENST00000679421.1:n.2214dup
ENST00000679459.1:c.985dup ENSP00000506137.1:p.Ile329AsnfsTer14
ENST00000679478.1:c.715dup ENSP00000506484.1:p.Ile239AsnfsTer14
ENST00000679639.1:n.788dup
ENST00000679994.1:c.715dup ENSP00000504957.1:p.Ile239AsnfsTer14
ENST00000680028.1:n.2349dup
ENST00000680155.1:c.715dup ENSP00000505333.1:p.Ile239AsnfsTer14
ENST00000680705.1:n.1029dup
ENST00000680770.1:c.985dup ENSP00000505536.1:p.Ile329AsnfsTer14
ENST00000680893.1:c.*233dup ENSP00000505929.1:n.*233dup
ENST00000680910.1:n.1015dup
ENST00000681028.1:c.715dup ENSP00000506323.1:p.Ile239AsnfsTer14
ENST00000681032.1:c.*363dup ENSP00000505205.1:n.*363dup
ENST00000681449.1:c.715dup ENSP00000505342.1:p.Ile239AsnfsTer14
ENST00000681565.1:c.985dup ENSP00000505620.1:p.Ile329AsnfsTer9
ENST00000681752.1:c.*755dup ENSP00000504994.1:n.*755dup
ENST00000681891.1:n.4729dup
ENST00000264167.8:c.985dup ENSP00000264167.4:p.Ile329AsnfsTer14
ENST00000409888.1:c.350+41649dup ENSP00000386688.1:n.350+41649dup
NM_003659.3:c.985dup NP_003650.1:p.Ile329AsnfsTer14
XM_011512041.1:c.715dup XP_011510343.1:p.Ile239AsnfsTer14
XM_011512042.1:c.715dup XP_011510344.1:p.Ile239AsnfsTer14
XM_011512043.1:c.250dup XP_011510345.1:p.Ile84AsnfsTer14
XM_011512044.1:c.985dup XP_011510346.1:p.Ile329AsnfsTer9
XM_011512045.1:c.985dup XP_011510347.1:p.Ile329AsnfsTer?
XM_011512041.2:c.715dup XP_011510343.1:p.Ile239AsnfsTer14
XM_011512043.2:c.250dup XP_011510345.1:p.Ile84AsnfsTer14
XR_001739007.2:n.1002dup
NM_003659.4:c.985dup MANE Select NP_003650.1:p.Ile329AsnfsTer14