Canonical Allele Identifier: CA351112949

Gene: PAX3

Linked Data

• MyVariant Identifiers: chr2:g.223096997C>T (hg19) ; chr2:g.222232278C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222232278C>T , CM000664.2:g.222232278C>T	GRCh38
NC_000002.11:g.223096997C>T , CM000664.1:g.223096997C>T	GRCh37
NC_000002.10:g.222805241C>T	NCBI36
NG_011632.1:g.71704G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336840.11:c.592G>A	ENSP00000338767.5:p.Ala198Thr
ENST00000344493.9:c.592G>A	ENSP00000342092.4:p.Ala198Thr
ENST00000350526.9:c.592G>A	ENSP00000343052.4:p.Ala198Thr
ENST00000392070.7:c.592G>A MANE Select	ENSP00000375922.3:p.Ala198Thr
ENST00000646154.1:n.406G>A
ENST00000336840.10:c.592G>A	ENSP00000338767.5:p.Ala198Thr
ENST00000344493.8:c.592G>A	ENSP00000342092.4:p.Ala198Thr
ENST00000350526.8:c.592G>A	ENSP00000343052.4:p.Ala198Thr
ENST00000392069.6:c.592G>A	ENSP00000375921.2:p.Ala198Thr
ENST00000392070.6:c.592G>A	ENSP00000375922.2:p.Ala198Thr
ENST00000409551.7:c.589G>A	ENSP00000386750.3:p.Ala197Thr
NM_001127366.2:c.589G>A	NP_001120838.1:p.Ala197Thr
NM_181457.3:c.592G>A	NP_852122.1:p.Ala198Thr
NM_181458.3:c.592G>A	NP_852123.1:p.Ala198Thr
NM_181459.3:c.592G>A	NP_852124.1:p.Ala198Thr
NM_181460.3:c.592G>A	NP_852125.1:p.Ala198Thr
NM_181461.3:c.592G>A	NP_852126.1:p.Ala198Thr
XM_011511278.1:c.736G>A	XP_011509580.1:p.Ala246Thr
XM_011511279.1:c.28G>A	XP_011509581.1:p.Ala10Thr
XR_923945.1:n.287+10308C>T
NM_001127366.3:c.589G>A	NP_001120838.1:p.Ala197Thr
NM_181457.4:c.592G>A	NP_852122.1:p.Ala198Thr
NM_181458.4:c.592G>A MANE Select	NP_852123.1:p.Ala198Thr
NM_181459.4:c.592G>A	NP_852124.1:p.Ala198Thr
NM_181460.4:c.592G>A	NP_852125.1:p.Ala198Thr
NM_181461.4:c.592G>A	NP_852126.1:p.Ala198Thr