Canonical Allele Identifier: CA1042721557
Gene: PAX3 HGNC NCBI

Linked Data

dbSNP Id: rs1692608772

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222231879del , CM000664.2:g.222231879del GRCh38
NC_000002.11:g.223096598del , CM000664.1:g.223096598del GRCh37
NC_000002.10:g.222804842del NCBI36
NG_011632.1:g.72104del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336840.11:c.792+200del ENSP00000338767.5:n.792+200del
ENST00000344493.9:c.792+200del ENSP00000342092.4:n.792+200del
ENST00000350526.9:c.792+200del ENSP00000343052.4:n.792+200del
ENST00000392070.7:c.792+200del MANE Select ENSP00000375922.3:n.792+200del
ENST00000646154.1:n.606+200del
ENST00000336840.10:c.792+200del ENSP00000338767.5:n.792+200del
ENST00000344493.8:c.792+200del ENSP00000342092.4:n.792+200del
ENST00000350526.8:c.792+200del ENSP00000343052.4:n.792+200del
ENST00000392069.6:c.792+200del ENSP00000375921.2:n.792+200del
ENST00000392070.6:c.792+200del ENSP00000375922.2:n.792+200del
ENST00000409551.7:c.789+200del ENSP00000386750.3:n.789+200del
NM_001127366.2:c.789+200del NP_001120838.1:n.789+200del
NM_181457.3:c.792+200del NP_852122.1:n.792+200del
NM_181458.3:c.792+200del NP_852123.1:n.792+200del
NM_181459.3:c.792+200del NP_852124.1:n.792+200del
NM_181460.3:c.792+200del NP_852125.1:n.792+200del
NM_181461.3:c.792+200del NP_852126.1:n.792+200del
XM_011511278.1:c.936+200del XP_011509580.1:n.936+200del
XM_011511279.1:c.228+200del XP_011509581.1:n.228+200del
XR_923945.1:n.287+9909del
XR_923946.1:n.288-133del
NM_001127366.3:c.789+200del NP_001120838.1:n.789+200del
NM_181457.4:c.792+200del NP_852122.1:n.792+200del
NM_181458.4:c.792+200del MANE Select NP_852123.1:n.792+200del
NM_181459.4:c.792+200del NP_852124.1:n.792+200del
NM_181460.4:c.792+200del NP_852125.1:n.792+200del
NM_181461.4:c.792+200del NP_852126.1:n.792+200del