Canonical Allele Identifier: CA913190011

Gene: PAX3

Linked Data

• ClinVar Variation Id: 4211
• ClinVar RCV Id: RCV000004431
• dbSNP Id: rs1559318562

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222295611_222295615del , CM000664.2:g.222295611_222295615del	GRCh38
NC_000002.11:g.223160330_223160334del , CM000664.1:g.223160330_223160334del	GRCh37
NC_000002.10:g.222868574_222868578del	NCBI36
NG_011632.1:g.8368_8372del
NG_021186.1:g.2465_2469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258387.6:c.365_369del	ENSP00000258387.5:p.Lys122ArgfsTer21
ENST00000336840.11:c.365_369del	ENSP00000338767.5:p.Lys122ArgfsTer21
ENST00000344493.9:c.365_369del	ENSP00000342092.4:p.Lys122ArgfsTer21
ENST00000350526.9:c.365_369del	ENSP00000343052.4:p.Lys122ArgfsTer21
ENST00000392070.7:c.365_369del MANE Select	ENSP00000375922.3:p.Lys122ArgfsTer21
ENST00000647467.1:n.746_750del
ENST00000258387.5:c.365_369del	ENSP00000258387.5:p.Lys122ArgfsTer21
ENST00000336840.10:c.365_369del	ENSP00000338767.5:p.Lys122ArgfsTer21
ENST00000344493.8:c.365_369del	ENSP00000342092.4:p.Lys122ArgfsTer21
ENST00000350526.8:c.365_369del	ENSP00000343052.4:p.Lys122ArgfsTer21
ENST00000392069.6:c.365_369del	ENSP00000375921.2:p.Lys122ArgfsTer21
ENST00000392070.6:c.365_369del	ENSP00000375922.2:p.Lys122ArgfsTer21
ENST00000409551.7:c.362_366del	ENSP00000386750.3:p.Lys121ArgfsTer21
ENST00000409828.7:c.365_369del	ENSP00000386817.3:p.Lys122ArgfsTer21
NM_000438.5:c.365_369del	NP_000429.2:p.Lys122ArgfsTer21
NM_001127366.2:c.362_366del	NP_001120838.1:p.Lys121ArgfsTer21
NM_013942.4:c.365_369del	NP_039230.1:p.Lys122ArgfsTer21
NM_181457.3:c.365_369del	NP_852122.1:p.Lys122ArgfsTer21
NM_181458.3:c.365_369del	NP_852123.1:p.Lys122ArgfsTer21
NM_181459.3:c.365_369del	NP_852124.1:p.Lys122ArgfsTer21
NM_181460.3:c.365_369del	NP_852125.1:p.Lys122ArgfsTer21
NM_181461.3:c.365_369del	NP_852126.1:p.Lys122ArgfsTer21
XM_011511278.1:c.509_513del	XP_011509580.1:p.Lys170ArgfsTer21
XM_011511280.1:c.509_513del	XP_011509582.1:p.Lys170ArgfsTer21
XM_011511281.1:c.509_513del	XP_011509583.1:p.Lys170ArgfsTer21
NM_000438.6:c.365_369del	NP_000429.2:p.Lys122ArgfsTer21
NM_001127366.3:c.362_366del	NP_001120838.1:p.Lys121ArgfsTer21
NM_013942.5:c.365_369del	NP_039230.1:p.Lys122ArgfsTer21
NM_181457.4:c.365_369del	NP_852122.1:p.Lys122ArgfsTer21
NM_181458.4:c.365_369del MANE Select	NP_852123.1:p.Lys122ArgfsTer21
NM_181459.4:c.365_369del	NP_852124.1:p.Lys122ArgfsTer21
NM_181460.4:c.365_369del	NP_852125.1:p.Lys122ArgfsTer21
NM_181461.4:c.365_369del	NP_852126.1:p.Lys122ArgfsTer21