Canonical Allele Identifier: CA1330502570

Gene: PAX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222201923C= , CM000664.2:g.222201923C=	GRCh38
NC_000002.11:g.223066642C= , CM000664.1:g.223066642C=	GRCh37
NC_000002.10:g.222774886C=	NCBI36
NG_011632.1:g.102059G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.1174-481G=	ENSP00000338767.5:n.1174-481G=
ENST00000344493.9:c.1174-481G=	ENSP00000342092.4:n.1174-481G=
ENST00000350526.9:c.*1G=	ENSP00000343052.4:n.*1G=
ENST00000392070.7:c.1420+21G= MANE Select	ENSP00000375922.3:n.1420+21G=
ENST00000464706.6:n.858+21G=
ENST00000644699.1:n.746+21G=
ENST00000646154.1:n.1234+21G=
ENST00000336840.10:c.1174-481G=	ENSP00000338767.5:n.1174-481G=
ENST00000344493.8:c.1174-481G=	ENSP00000342092.4:n.1174-481G=
ENST00000350526.8:c.*1G=	ENSP00000343052.4:n.*1G=
ENST00000392069.6:c.1420+21G=	ENSP00000375921.2:n.1420+21G=
ENST00000392070.6:c.1420+21G=	ENSP00000375922.2:n.1420+21G=
ENST00000409551.7:c.1417+21G=	ENSP00000386750.3:n.1417+21G=
NM_001127366.2:c.1417+21G=	NP_001120838.1:n.1417+21G=
NM_181457.3:c.*1G=	NP_852122.1:n.*1G=
NM_181458.3:c.1420+21G=	NP_852123.1:n.1420+21G=
NM_181459.3:c.1420+21G=	NP_852124.1:n.1420+21G=
NM_181460.3:c.1174-481G=	NP_852125.1:n.1174-481G=
NM_181461.3:c.1174-481G=	NP_852126.1:n.1174-481G=
XM_011511278.1:c.1564+21G=	XP_011509580.1:n.1564+21G=
XM_011511279.1:c.856+21G=	XP_011509581.1:n.856+21G=
NM_001127366.3:c.1417+21G=	NP_001120838.1:n.1417+21G=
NM_181457.4:c.*1G=	NP_852122.1:n.*1G=
NM_181458.4:c.1420+21G= MANE Select	NP_852123.1:n.1420+21G=
NM_181459.4:c.1420+21G=	NP_852124.1:n.1420+21G=
NM_181460.4:c.1174-481G=	NP_852125.1:n.1174-481G=
NM_181461.4:c.1174-481G=	NP_852126.1:n.1174-481G=