Canonical Allele Identifier: CA339658
Gene: PAX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 218940
dbSNP Id: rs2234675

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222221236G>T , CM000664.2:g.222221236G>T GRCh38
NC_000002.11:g.223085955G>T , CM000664.1:g.223085955G>T GRCh37
NC_000002.10:g.222794199G>T NCBI36
NG_011632.1:g.82746C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000336840.11:c.944C>A ENSP00000338767.5:p.Thr315Lys
ENST00000344493.9:c.944C>A ENSP00000342092.4:p.Thr315Lys
ENST00000350526.9:c.944C>A ENSP00000343052.4:p.Thr315Lys
ENST00000392070.7:c.944C>A MANE Select ENSP00000375922.3:p.Thr315Lys
ENST00000464706.6:n.382C>A
ENST00000644699.1:n.270C>A
ENST00000644937.1:n.216C>A
ENST00000646154.1:n.758C>A
ENST00000336840.10:c.944C>A ENSP00000338767.5:p.Thr315Lys
ENST00000344493.8:c.944C>A ENSP00000342092.4:p.Thr315Lys
ENST00000350526.8:c.944C>A ENSP00000343052.4:p.Thr315Lys
ENST00000392069.6:c.944C>A ENSP00000375921.2:p.Thr315Lys
ENST00000392070.6:c.944C>A ENSP00000375922.2:p.Thr315Lys
ENST00000409551.7:c.941C>A ENSP00000386750.3:p.Thr314Lys
ENST00000464706.5:n.368C>A
ENST00000555548.1:n.175C>A
NM_001127366.2:c.941C>A NP_001120838.1:p.Thr314Lys
NM_181457.3:c.944C>A NP_852122.1:p.Thr315Lys
NM_181458.3:c.944C>A NP_852123.1:p.Thr315Lys
NM_181459.3:c.944C>A NP_852124.1:p.Thr315Lys
NM_181460.3:c.944C>A NP_852125.1:p.Thr315Lys
NM_181461.3:c.944C>A NP_852126.1:p.Thr315Lys
XM_011511278.1:c.1088C>A XP_011509580.1:p.Thr363Lys
XM_011511279.1:c.380C>A XP_011509581.1:p.Thr127Lys
NM_001127366.3:c.941C>A NP_001120838.1:p.Thr314Lys
NM_181457.4:c.944C>A NP_852122.1:p.Thr315Lys
NM_181458.4:c.944C>A MANE Select NP_852123.1:p.Thr315Lys
NM_181459.4:c.944C>A NP_852124.1:p.Thr315Lys
NM_181460.4:c.944C>A NP_852125.1:p.Thr315Lys
NM_181461.4:c.944C>A NP_852126.1:p.Thr315Lys