Canonical Allele Identifier: CA2135497
Gene: PAX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 334559
dbSNP Id: rs200701839

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222220195G>A , CM000664.2:g.222220195G>A GRCh38
NC_000002.11:g.223084914G>A , CM000664.1:g.223084914G>A GRCh37
NC_000002.10:g.222793158G>A NCBI36
NG_011632.1:g.83787C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336840.11:c.1118C>T ENSP00000338767.5:p.Pro373Leu
ENST00000344493.9:c.1118C>T ENSP00000342092.4:p.Pro373Leu
ENST00000350526.9:c.1118C>T ENSP00000343052.4:p.Pro373Leu
ENST00000392070.7:c.1118C>T MANE Select ENSP00000375922.3:p.Pro373Leu
ENST00000464706.6:n.556C>T
ENST00000644699.1:n.444C>T
ENST00000644937.1:n.390C>T
ENST00000646154.1:n.932C>T
ENST00000336840.10:c.1118C>T ENSP00000338767.5:p.Pro373Leu
ENST00000344493.8:c.1118C>T ENSP00000342092.4:p.Pro373Leu
ENST00000350526.8:c.1118C>T ENSP00000343052.4:p.Pro373Leu
ENST00000392069.6:c.1118C>T ENSP00000375921.2:p.Pro373Leu
ENST00000392070.6:c.1118C>T ENSP00000375922.2:p.Pro373Leu
ENST00000409551.7:c.1115C>T ENSP00000386750.3:p.Pro372Leu
ENST00000464706.5:n.542C>T
ENST00000555548.1:n.349C>T
NM_001127366.2:c.1115C>T NP_001120838.1:p.Pro372Leu
NM_181457.3:c.1118C>T NP_852122.1:p.Pro373Leu
NM_181458.3:c.1118C>T NP_852123.1:p.Pro373Leu
NM_181459.3:c.1118C>T NP_852124.1:p.Pro373Leu
NM_181460.3:c.1118C>T NP_852125.1:p.Pro373Leu
NM_181461.3:c.1118C>T NP_852126.1:p.Pro373Leu
XM_011511278.1:c.1262C>T XP_011509580.1:p.Pro421Leu
XM_011511279.1:c.554C>T XP_011509581.1:p.Pro185Leu
XR_001739903.1:n.240-201G>A
NM_001127366.3:c.1115C>T NP_001120838.1:p.Pro372Leu
NM_181457.4:c.1118C>T NP_852122.1:p.Pro373Leu
NM_181458.4:c.1118C>T MANE Select NP_852123.1:p.Pro373Leu
NM_181459.4:c.1118C>T NP_852124.1:p.Pro373Leu
NM_181460.4:c.1118C>T NP_852125.1:p.Pro373Leu
NM_181461.4:c.1118C>T NP_852126.1:p.Pro373Leu