Canonical Allele Identifier: CA1330516273

Gene: PAX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222232280G= , CM000664.2:g.222232280G=	GRCh38
NC_000002.11:g.223096999G= , CM000664.1:g.223096999G=	GRCh37
NC_000002.10:g.222805243G=	NCBI36
NG_011632.1:g.71702C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000336840.11:c.590C=	ENSP00000338767.5:p.Ser197=
ENST00000344493.9:c.590C=	ENSP00000342092.4:p.Ser197=
ENST00000350526.9:c.590C=	ENSP00000343052.4:p.Ser197=
ENST00000392070.7:c.590C= MANE Select	ENSP00000375922.3:p.Ser197=
ENST00000646154.1:n.404C=
ENST00000336840.10:c.590C=	ENSP00000338767.5:p.Ser197=
ENST00000344493.8:c.590C=	ENSP00000342092.4:p.Ser197=
ENST00000350526.8:c.590C=	ENSP00000343052.4:p.Ser197=
ENST00000392069.6:c.590C=	ENSP00000375921.2:p.Ser197=
ENST00000392070.6:c.590C=	ENSP00000375922.2:p.Ser197=
ENST00000409551.7:c.587C=	ENSP00000386750.3:p.Ser196=
NM_001127366.2:c.587C=	NP_001120838.1:p.Ser196=
NM_181457.3:c.590C=	NP_852122.1:p.Ser197=
NM_181458.3:c.590C=	NP_852123.1:p.Ser197=
NM_181459.3:c.590C=	NP_852124.1:p.Ser197=
NM_181460.3:c.590C=	NP_852125.1:p.Ser197=
NM_181461.3:c.590C=	NP_852126.1:p.Ser197=
XM_011511278.1:c.734C=	XP_011509580.1:p.Ser245=
XM_011511279.1:c.26C=	XP_011509581.1:p.Ser9=
XR_923945.1:n.287+10310G=
NM_001127366.3:c.587C=	NP_001120838.1:p.Ser196=
NM_181457.4:c.590C=	NP_852122.1:p.Ser197=
NM_181458.4:c.590C= MANE Select	NP_852123.1:p.Ser197=
NM_181459.4:c.590C=	NP_852124.1:p.Ser197=
NM_181460.4:c.590C=	NP_852125.1:p.Ser197=
NM_181461.4:c.590C=	NP_852126.1:p.Ser197=