Canonical Allele Identifier: CA351113327
Gene: PAX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222295656T>C , CM000664.2:g.222295656T>C GRCh38
NC_000002.11:g.223160375T>C , CM000664.1:g.223160375T>C GRCh37
NC_000002.10:g.222868619T>C NCBI36
NG_011632.1:g.8326A>G
NG_021186.1:g.2510T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258387.6:c.323A>G ENSP00000258387.5:p.Gln108Arg
ENST00000336840.11:c.323A>G ENSP00000338767.5:p.Gln108Arg
ENST00000344493.9:c.323A>G ENSP00000342092.4:p.Gln108Arg
ENST00000350526.9:c.323A>G ENSP00000343052.4:p.Gln108Arg
ENST00000392070.7:c.323A>G MANE Select ENSP00000375922.3:p.Gln108Arg
ENST00000647467.1:n.704A>G
ENST00000258387.5:c.323A>G ENSP00000258387.5:p.Gln108Arg
ENST00000336840.10:c.323A>G ENSP00000338767.5:p.Gln108Arg
ENST00000344493.8:c.323A>G ENSP00000342092.4:p.Gln108Arg
ENST00000350526.8:c.323A>G ENSP00000343052.4:p.Gln108Arg
ENST00000392069.6:c.323A>G ENSP00000375921.2:p.Gln108Arg
ENST00000392070.6:c.323A>G ENSP00000375922.2:p.Gln108Arg
ENST00000409551.7:c.322-2A>G ENSP00000386750.3:n.322-2A>G
ENST00000409828.7:c.323A>G ENSP00000386817.3:p.Gln108Arg
NM_000438.5:c.323A>G NP_000429.2:p.Gln108Arg
NM_001127366.2:c.322-2A>G NP_001120838.1:n.322-2A>G
NM_013942.4:c.323A>G NP_039230.1:p.Gln108Arg
NM_181457.3:c.323A>G NP_852122.1:p.Gln108Arg
NM_181458.3:c.323A>G NP_852123.1:p.Gln108Arg
NM_181459.3:c.323A>G NP_852124.1:p.Gln108Arg
NM_181460.3:c.323A>G NP_852125.1:p.Gln108Arg
NM_181461.3:c.323A>G NP_852126.1:p.Gln108Arg
XM_011511278.1:c.467A>G XP_011509580.1:p.Gln156Arg
XM_011511280.1:c.467A>G XP_011509582.1:p.Gln156Arg
XM_011511281.1:c.467A>G XP_011509583.1:p.Gln156Arg
NM_000438.6:c.323A>G NP_000429.2:p.Gln108Arg
NM_001127366.3:c.322-2A>G NP_001120838.1:n.322-2A>G
NM_013942.5:c.323A>G NP_039230.1:p.Gln108Arg
NM_181457.4:c.323A>G NP_852122.1:p.Gln108Arg
NM_181458.4:c.323A>G MANE Select NP_852123.1:p.Gln108Arg
NM_181459.4:c.323A>G NP_852124.1:p.Gln108Arg
NM_181460.4:c.323A>G NP_852125.1:p.Gln108Arg
NM_181461.4:c.323A>G NP_852126.1:p.Gln108Arg