Canonical Allele Identifier: CA2663324225
Gene: PAX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222297345_222297350del , CM000664.2:g.222297345_222297350del GRCh38
NC_000002.11:g.223162064_223162069del , CM000664.1:g.223162064_223162069del GRCh37
NC_000002.10:g.222870308_222870313del NCBI36
NG_011632.1:g.6635_6640del
NG_021186.1:g.4199_4204del

Transcript Alleles

HGVS Amino-acid Change
ENST00000258387.6:c.86-134_86-129del ENSP00000258387.5:n.86-134_86-129del
ENST00000336840.11:c.86-134_86-129del ENSP00000338767.5:n.86-134_86-129del
ENST00000344493.9:c.86-134_86-129del ENSP00000342092.4:n.86-134_86-129del
ENST00000350526.9:c.86-134_86-129del ENSP00000343052.4:n.86-134_86-129del
ENST00000392070.7:c.86-134_86-129del MANE Select ENSP00000375922.3:n.86-134_86-129del
ENST00000647467.1:n.467-134_467-129del
ENST00000258387.5:c.86-134_86-129del ENSP00000258387.5:n.86-134_86-129del
ENST00000336840.10:c.86-134_86-129del ENSP00000338767.5:n.86-134_86-129del
ENST00000344493.8:c.86-134_86-129del ENSP00000342092.4:n.86-134_86-129del
ENST00000350526.8:c.86-134_86-129del ENSP00000343052.4:n.86-134_86-129del
ENST00000392069.6:c.86-134_86-129del ENSP00000375921.2:n.86-134_86-129del
ENST00000392070.6:c.86-134_86-129del ENSP00000375922.2:n.86-134_86-129del
ENST00000409551.7:c.86-134_86-129del ENSP00000386750.3:n.86-134_86-129del
ENST00000409828.7:c.86-134_86-129del ENSP00000386817.3:n.86-134_86-129del
NM_000438.5:c.86-134_86-129del NP_000429.2:n.86-134_86-129del
NM_001127366.2:c.86-134_86-129del NP_001120838.1:n.86-134_86-129del
NM_013942.4:c.86-134_86-129del NP_039230.1:n.86-134_86-129del
NM_181457.3:c.86-134_86-129del NP_852122.1:n.86-134_86-129del
NM_181458.3:c.86-134_86-129del NP_852123.1:n.86-134_86-129del
NM_181459.3:c.86-134_86-129del NP_852124.1:n.86-134_86-129del
NM_181460.3:c.86-134_86-129del NP_852125.1:n.86-134_86-129del
NM_181461.3:c.86-134_86-129del NP_852126.1:n.86-134_86-129del
XM_011511278.1:c.230-134_230-129del XP_011509580.1:n.230-134_230-129del
XM_011511280.1:c.230-134_230-129del XP_011509582.1:n.230-134_230-129del
XM_011511281.1:c.230-134_230-129del XP_011509583.1:n.230-134_230-129del
NM_000438.6:c.86-134_86-129del NP_000429.2:n.86-134_86-129del
NM_001127366.3:c.86-134_86-129del NP_001120838.1:n.86-134_86-129del
NM_013942.5:c.86-134_86-129del NP_039230.1:n.86-134_86-129del
NM_181457.4:c.86-134_86-129del NP_852122.1:n.86-134_86-129del
NM_181458.4:c.86-134_86-129del MANE Select NP_852123.1:n.86-134_86-129del
NM_181459.4:c.86-134_86-129del NP_852124.1:n.86-134_86-129del
NM_181460.4:c.86-134_86-129del NP_852125.1:n.86-134_86-129del
NM_181461.4:c.86-134_86-129del NP_852126.1:n.86-134_86-129del