Canonical Allele Identifier: CA351115854
Gene: PAX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222202151G>T , CM000664.2:g.222202151G>T GRCh38
NC_000002.11:g.223066870G>T , CM000664.1:g.223066870G>T GRCh37
NC_000002.10:g.222775114G>T NCBI36
NG_011632.1:g.101831C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336840.11:c.1174-709C>A ENSP00000338767.5:n.1174-709C>A
ENST00000344493.9:c.1174-709C>A ENSP00000342092.4:n.1174-709C>A
ENST00000350526.9:c.1213C>A ENSP00000343052.4:p.Gln405Lys
ENST00000392070.7:c.1213C>A MANE Select ENSP00000375922.3:p.Gln405Lys
ENST00000464706.6:n.651C>A
ENST00000644699.1:n.539C>A
ENST00000646154.1:n.1027C>A
ENST00000336840.10:c.1174-709C>A ENSP00000338767.5:n.1174-709C>A
ENST00000344493.8:c.1174-709C>A ENSP00000342092.4:n.1174-709C>A
ENST00000350526.8:c.1213C>A ENSP00000343052.4:p.Gln405Lys
ENST00000392069.6:c.1213C>A ENSP00000375921.2:p.Gln405Lys
ENST00000392070.6:c.1213C>A ENSP00000375922.2:p.Gln405Lys
ENST00000409551.7:c.1210C>A ENSP00000386750.3:p.Gln404Lys
ENST00000464706.5:n.637C>A
ENST00000555548.1:n.444C>A
NM_001127366.2:c.1210C>A NP_001120838.1:p.Gln404Lys
NM_181457.3:c.1213C>A NP_852122.1:p.Gln405Lys
NM_181458.3:c.1213C>A NP_852123.1:p.Gln405Lys
NM_181459.3:c.1213C>A NP_852124.1:p.Gln405Lys
NM_181460.3:c.1174-709C>A NP_852125.1:n.1174-709C>A
NM_181461.3:c.1174-709C>A NP_852126.1:n.1174-709C>A
XM_011511278.1:c.1357C>A XP_011509580.1:p.Gln453Lys
XM_011511279.1:c.649C>A XP_011509581.1:p.Gln217Lys
NM_001127366.3:c.1210C>A NP_001120838.1:p.Gln404Lys
NM_181457.4:c.1213C>A NP_852122.1:p.Gln405Lys
NM_181458.4:c.1213C>A MANE Select NP_852123.1:p.Gln405Lys
NM_181459.4:c.1213C>A NP_852124.1:p.Gln405Lys
NM_181460.4:c.1174-709C>A NP_852125.1:n.1174-709C>A
NM_181461.4:c.1174-709C>A NP_852126.1:n.1174-709C>A