Canonical Allele Identifier: CA351112156

Gene: PAX3

Linked Data

• MyVariant Identifiers: chr2:g.223096808C>G (hg19) ; chr2:g.222232089C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222232089C>G , CM000664.2:g.222232089C>G	GRCh38
NC_000002.11:g.223096808C>G , CM000664.1:g.223096808C>G	GRCh37
NC_000002.10:g.222805052C>G	NCBI36
NG_011632.1:g.71893G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.781G>C	ENSP00000338767.5:p.Ala261Pro
ENST00000344493.9:c.781G>C	ENSP00000342092.4:p.Ala261Pro
ENST00000350526.9:c.781G>C	ENSP00000343052.4:p.Ala261Pro
ENST00000392070.7:c.781G>C MANE Select	ENSP00000375922.3:p.Ala261Pro
ENST00000646154.1:n.595G>C
ENST00000336840.10:c.781G>C	ENSP00000338767.5:p.Ala261Pro
ENST00000344493.8:c.781G>C	ENSP00000342092.4:p.Ala261Pro
ENST00000350526.8:c.781G>C	ENSP00000343052.4:p.Ala261Pro
ENST00000392069.6:c.781G>C	ENSP00000375921.2:p.Ala261Pro
ENST00000392070.6:c.781G>C	ENSP00000375922.2:p.Ala261Pro
ENST00000409551.7:c.778G>C	ENSP00000386750.3:p.Ala260Pro
NM_001127366.2:c.778G>C	NP_001120838.1:p.Ala260Pro
NM_181457.3:c.781G>C	NP_852122.1:p.Ala261Pro
NM_181458.3:c.781G>C	NP_852123.1:p.Ala261Pro
NM_181459.3:c.781G>C	NP_852124.1:p.Ala261Pro
NM_181460.3:c.781G>C	NP_852125.1:p.Ala261Pro
NM_181461.3:c.781G>C	NP_852126.1:p.Ala261Pro
XM_011511278.1:c.925G>C	XP_011509580.1:p.Ala309Pro
XM_011511279.1:c.217G>C	XP_011509581.1:p.Ala73Pro
XR_923945.1:n.287+10119C>G
XR_923946.1:n.365C>G
NM_001127366.3:c.778G>C	NP_001120838.1:p.Ala260Pro
NM_181457.4:c.781G>C	NP_852122.1:p.Ala261Pro
NM_181458.4:c.781G>C MANE Select	NP_852123.1:p.Ala261Pro
NM_181459.4:c.781G>C	NP_852124.1:p.Ala261Pro
NM_181460.4:c.781G>C	NP_852125.1:p.Ala261Pro
NM_181461.4:c.781G>C	NP_852126.1:p.Ala261Pro