Canonical Allele Identifier: CA2135479

Gene: PAX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222220100G>A , CM000664.2:g.222220100G>A	GRCh38
NC_000002.11:g.223084819G>A , CM000664.1:g.223084819G>A	GRCh37
NC_000002.10:g.222793063G>A	NCBI36
NG_011632.1:g.83882C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.1173+40C>T	ENSP00000338767.5:n.1173+40C>T
ENST00000344493.9:c.1173+40C>T	ENSP00000342092.4:n.1173+40C>T
ENST00000350526.9:c.1173+40C>T	ENSP00000343052.4:n.1173+40C>T
ENST00000392070.7:c.1173+40C>T MANE Select	ENSP00000375922.3:n.1173+40C>T
ENST00000464706.6:n.611+40C>T
ENST00000644699.1:n.499+40C>T
ENST00000644937.1:n.445+40C>T
ENST00000646154.1:n.987+40C>T
ENST00000336840.10:c.1173+40C>T	ENSP00000338767.5:n.1173+40C>T
ENST00000344493.8:c.1173+40C>T	ENSP00000342092.4:n.1173+40C>T
ENST00000350526.8:c.1173+40C>T	ENSP00000343052.4:n.1173+40C>T
ENST00000392069.6:c.1173+40C>T	ENSP00000375921.2:n.1173+40C>T
ENST00000392070.6:c.1173+40C>T	ENSP00000375922.2:n.1173+40C>T
ENST00000409551.7:c.1170+40C>T	ENSP00000386750.3:n.1170+40C>T
ENST00000464706.5:n.597+40C>T
ENST00000555548.1:n.404+40C>T
NM_001127366.2:c.1170+40C>T	NP_001120838.1:n.1170+40C>T
NM_181457.3:c.1173+40C>T	NP_852122.1:n.1173+40C>T
NM_181458.3:c.1173+40C>T	NP_852123.1:n.1173+40C>T
NM_181459.3:c.1173+40C>T	NP_852124.1:n.1173+40C>T
NM_181460.3:c.1173+40C>T	NP_852125.1:n.1173+40C>T
NM_181461.3:c.1173+40C>T	NP_852126.1:n.1173+40C>T
XM_011511278.1:c.1317+40C>T	XP_011509580.1:n.1317+40C>T
XM_011511279.1:c.609+40C>T	XP_011509581.1:n.609+40C>T
XR_001739903.1:n.240-296G>A
NM_001127366.3:c.1170+40C>T	NP_001120838.1:n.1170+40C>T
NM_181457.4:c.1173+40C>T	NP_852122.1:n.1173+40C>T
NM_181458.4:c.1173+40C>T MANE Select	NP_852123.1:n.1173+40C>T
NM_181459.4:c.1173+40C>T	NP_852124.1:n.1173+40C>T
NM_181460.4:c.1173+40C>T	NP_852125.1:n.1173+40C>T
NM_181461.4:c.1173+40C>T	NP_852126.1:n.1173+40C>T