Canonical Allele Identifier: CA1330516249

Gene: PAX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222232202C= , CM000664.2:g.222232202C=	GRCh38
NC_000002.11:g.223096921C= , CM000664.1:g.223096921C=	GRCh37
NC_000002.10:g.222805165C=	NCBI36
NG_011632.1:g.71780G=

Transcript Alleles

HGVS	Amino-acid Change
NM_181458.4:c.668G= MANE Select	NP_852123.1:p.Arg223=
ENST00000392070.7:c.668G= MANE Select	ENSP00000375922.3:p.Arg223=
NM_001127366.2:c.665G=	NP_001120838.1:p.Arg222=
NM_001127366.3:c.665G=	NP_001120838.1:p.Arg222=
NM_181457.3:c.668G=	NP_852122.1:p.Arg223=
NM_181457.4:c.668G=	NP_852122.1:p.Arg223=
NM_181458.3:c.668G=	NP_852123.1:p.Arg223=
NM_181459.3:c.668G=	NP_852124.1:p.Arg223=
NM_181459.4:c.668G=	NP_852124.1:p.Arg223=
NM_181460.3:c.668G=	NP_852125.1:p.Arg223=
NM_181460.4:c.668G=	NP_852125.1:p.Arg223=
NM_181461.3:c.668G=	NP_852126.1:p.Arg223=
NM_181461.4:c.668G=	NP_852126.1:p.Arg223=
ENST00000336840.10:c.668G=	ENSP00000338767.5:p.Arg223=
ENST00000336840.11:c.668G=	ENSP00000338767.5:p.Arg223=
ENST00000344493.8:c.668G=	ENSP00000342092.4:p.Arg223=
ENST00000344493.9:c.668G=	ENSP00000342092.4:p.Arg223=
ENST00000350526.8:c.668G=	ENSP00000343052.4:p.Arg223=
ENST00000350526.9:c.668G=	ENSP00000343052.4:p.Arg223=
ENST00000392069.6:c.668G=	ENSP00000375921.2:p.Arg223=
ENST00000392070.6:c.668G=	ENSP00000375922.2:p.Arg223=
ENST00000409551.7:c.665G=	ENSP00000386750.3:p.Arg222=
ENST00000646154.1:n.482G=
XM_011511278.1:c.812G=	XP_011509580.1:p.Arg271=
XM_011511279.1:c.104G=	XP_011509581.1:p.Arg35=
XR_923945.1:n.287+10232C=