Canonical Allele Identifier: CA2135749
Gene: PAX3 HGNC NCBI

Linked Data

dbSNP Id: rs748817593

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222295547A>G , CM000664.2:g.222295547A>G GRCh38
NC_000002.11:g.223160266A>G , CM000664.1:g.223160266A>G GRCh37
NC_000002.10:g.222868510A>G NCBI36
NG_011632.1:g.8435T>C
NG_021186.1:g.2401A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258387.6:c.432T>C ENSP00000258387.5:p.Asp144=
ENST00000336840.11:c.432T>C ENSP00000338767.5:p.Asp144=
ENST00000344493.9:c.432T>C ENSP00000342092.4:p.Asp144=
ENST00000350526.9:c.432T>C ENSP00000343052.4:p.Asp144=
ENST00000392070.7:c.432T>C MANE Select ENSP00000375922.3:p.Asp144=
ENST00000647467.1:n.813T>C
ENST00000258387.5:c.432T>C ENSP00000258387.5:p.Asp144=
ENST00000336840.10:c.432T>C ENSP00000338767.5:p.Asp144=
ENST00000344493.8:c.432T>C ENSP00000342092.4:p.Asp144=
ENST00000350526.8:c.432T>C ENSP00000343052.4:p.Asp144=
ENST00000392069.6:c.432T>C ENSP00000375921.2:p.Asp144=
ENST00000392070.6:c.432T>C ENSP00000375922.2:p.Asp144=
ENST00000409551.7:c.429T>C ENSP00000386750.3:p.Asp143=
ENST00000409828.7:c.432T>C ENSP00000386817.3:p.Asp144=
NM_000438.5:c.432T>C NP_000429.2:p.Asp144=
NM_001127366.2:c.429T>C NP_001120838.1:p.Asp143=
NM_013942.4:c.432T>C NP_039230.1:p.Asp144=
NM_181457.3:c.432T>C NP_852122.1:p.Asp144=
NM_181458.3:c.432T>C NP_852123.1:p.Asp144=
NM_181459.3:c.432T>C NP_852124.1:p.Asp144=
NM_181460.3:c.432T>C NP_852125.1:p.Asp144=
NM_181461.3:c.432T>C NP_852126.1:p.Asp144=
XM_011511278.1:c.576T>C XP_011509580.1:p.Asp192=
XM_011511280.1:c.576T>C XP_011509582.1:p.Asp192=
XM_011511281.1:c.576T>C XP_011509583.1:p.Asp192=
NM_000438.6:c.432T>C NP_000429.2:p.Asp144=
NM_001127366.3:c.429T>C NP_001120838.1:p.Asp143=
NM_013942.5:c.432T>C NP_039230.1:p.Asp144=
NM_181457.4:c.432T>C NP_852122.1:p.Asp144=
NM_181458.4:c.432T>C MANE Select NP_852123.1:p.Asp144=
NM_181459.4:c.432T>C NP_852124.1:p.Asp144=
NM_181460.4:c.432T>C NP_852125.1:p.Asp144=
NM_181461.4:c.432T>C NP_852126.1:p.Asp144=