Canonical Allele Identifier: CA2663324082

Gene: PAX3

Linked Data

• gnomAD v4: 2-222296937-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222296940_222296941del , CM000664.2:g.222296940_222296941del	GRCh38
NC_000002.11:g.223161659_223161660del , CM000664.1:g.223161659_223161660del	GRCh37
NC_000002.10:g.222869903_222869904del	NCBI36
NG_011632.1:g.7043_7044del
NG_021186.1:g.3794_3795del

Transcript Alleles

HGVS	Amino-acid change
ENST00000258387.6:c.321+39_321+40del	ENSP00000258387.5:n.321+39_321+40del
ENST00000336840.11:c.321+39_321+40del	ENSP00000338767.5:n.321+39_321+40del
ENST00000344493.9:c.321+39_321+40del	ENSP00000342092.4:n.321+39_321+40del
ENST00000350526.9:c.321+39_321+40del	ENSP00000343052.4:n.321+39_321+40del
ENST00000392070.7:c.321+39_321+40del MANE Select	ENSP00000375922.3:n.321+39_321+40del
ENST00000647467.1:n.702+39_702+40del
ENST00000258387.5:c.321+39_321+40del	ENSP00000258387.5:n.321+39_321+40del
ENST00000336840.10:c.321+39_321+40del	ENSP00000338767.5:n.321+39_321+40del
ENST00000344493.8:c.321+39_321+40del	ENSP00000342092.4:n.321+39_321+40del
ENST00000350526.8:c.321+39_321+40del	ENSP00000343052.4:n.321+39_321+40del
ENST00000392069.6:c.321+39_321+40del	ENSP00000375921.2:n.321+39_321+40del
ENST00000392070.6:c.321+39_321+40del	ENSP00000375922.2:n.321+39_321+40del
ENST00000409551.7:c.321+39_321+40del	ENSP00000386750.3:n.321+39_321+40del
ENST00000409828.7:c.321+39_321+40del	ENSP00000386817.3:n.321+39_321+40del
NM_000438.5:c.321+39_321+40del	NP_000429.2:n.321+39_321+40del
NM_001127366.2:c.321+39_321+40del	NP_001120838.1:n.321+39_321+40del
NM_013942.4:c.321+39_321+40del	NP_039230.1:n.321+39_321+40del
NM_181457.3:c.321+39_321+40del	NP_852122.1:n.321+39_321+40del
NM_181458.3:c.321+39_321+40del	NP_852123.1:n.321+39_321+40del
NM_181459.3:c.321+39_321+40del	NP_852124.1:n.321+39_321+40del
NM_181460.3:c.321+39_321+40del	NP_852125.1:n.321+39_321+40del
NM_181461.3:c.321+39_321+40del	NP_852126.1:n.321+39_321+40del
XM_011511278.1:c.465+39_465+40del	XP_011509580.1:n.465+39_465+40del
XM_011511280.1:c.465+39_465+40del	XP_011509582.1:n.465+39_465+40del
XM_011511281.1:c.465+39_465+40del	XP_011509583.1:n.465+39_465+40del
NM_000438.6:c.321+39_321+40del	NP_000429.2:n.321+39_321+40del
NM_001127366.3:c.321+39_321+40del	NP_001120838.1:n.321+39_321+40del
NM_013942.5:c.321+39_321+40del	NP_039230.1:n.321+39_321+40del
NM_181457.4:c.321+39_321+40del	NP_852122.1:n.321+39_321+40del
NM_181458.4:c.321+39_321+40del MANE Select	NP_852123.1:n.321+39_321+40del
NM_181459.4:c.321+39_321+40del	NP_852124.1:n.321+39_321+40del
NM_181460.4:c.321+39_321+40del	NP_852125.1:n.321+39_321+40del
NM_181461.4:c.321+39_321+40del	NP_852126.1:n.321+39_321+40del