Canonical Allele Identifier: CA1330516083

Gene: PAX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222231837G= , CM000664.2:g.222231837G=	GRCh38
NC_000002.11:g.223096556G= , CM000664.1:g.223096556G=	GRCh37
NC_000002.10:g.222804800G=	NCBI36
NG_011632.1:g.72145C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.792+241C=	ENSP00000338767.5:n.792+241C=
ENST00000344493.9:c.792+241C=	ENSP00000342092.4:n.792+241C=
ENST00000350526.9:c.792+241C=	ENSP00000343052.4:n.792+241C=
ENST00000392070.7:c.792+241C= MANE Select	ENSP00000375922.3:n.792+241C=
ENST00000646154.1:n.606+241C=
ENST00000336840.10:c.792+241C=	ENSP00000338767.5:n.792+241C=
ENST00000344493.8:c.792+241C=	ENSP00000342092.4:n.792+241C=
ENST00000350526.8:c.792+241C=	ENSP00000343052.4:n.792+241C=
ENST00000392069.6:c.792+241C=	ENSP00000375921.2:n.792+241C=
ENST00000392070.6:c.792+241C=	ENSP00000375922.2:n.792+241C=
ENST00000409551.7:c.789+241C=	ENSP00000386750.3:n.789+241C=
NM_001127366.2:c.789+241C=	NP_001120838.1:n.789+241C=
NM_181457.3:c.792+241C=	NP_852122.1:n.792+241C=
NM_181458.3:c.792+241C=	NP_852123.1:n.792+241C=
NM_181459.3:c.792+241C=	NP_852124.1:n.792+241C=
NM_181460.3:c.792+241C=	NP_852125.1:n.792+241C=
NM_181461.3:c.792+241C=	NP_852126.1:n.792+241C=
XM_011511278.1:c.936+241C=	XP_011509580.1:n.936+241C=
XM_011511279.1:c.228+241C=	XP_011509581.1:n.228+241C=
XR_923945.1:n.287+9867G=
XR_923946.1:n.288-175G=
NM_001127366.3:c.789+241C=	NP_001120838.1:n.789+241C=
NM_181457.4:c.792+241C=	NP_852122.1:n.792+241C=
NM_181458.4:c.792+241C= MANE Select	NP_852123.1:n.792+241C=
NM_181459.4:c.792+241C=	NP_852124.1:n.792+241C=
NM_181460.4:c.792+241C=	NP_852125.1:n.792+241C=
NM_181461.4:c.792+241C=	NP_852126.1:n.792+241C=