Canonical Allele Identifier: CA431575520

Gene: PAX3

Linked Data

• MyVariant Identifiers: chr2:g.223086011G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222221292G>T , CM000664.2:g.222221292G>T	GRCh38
NC_000002.11:g.223086011G>T , CM000664.1:g.223086011G>T	GRCh37
NC_000002.10:g.222794255G>T	NCBI36
NG_011632.1:g.82690C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.888C>A	ENSP00000338767.5:p.Pro296=
ENST00000344493.9:c.888C>A	ENSP00000342092.4:p.Pro296=
ENST00000350526.9:c.888C>A	ENSP00000343052.4:p.Pro296=
ENST00000392070.7:c.888C>A MANE Select	ENSP00000375922.3:p.Pro296=
ENST00000464706.6:n.326C>A
ENST00000644699.1:n.214C>A
ENST00000644937.1:n.160C>A
ENST00000646154.1:n.702C>A
ENST00000336840.10:c.888C>A	ENSP00000338767.5:p.Pro296=
ENST00000344493.8:c.888C>A	ENSP00000342092.4:p.Pro296=
ENST00000350526.8:c.888C>A	ENSP00000343052.4:p.Pro296=
ENST00000392069.6:c.888C>A	ENSP00000375921.2:p.Pro296=
ENST00000392070.6:c.888C>A	ENSP00000375922.2:p.Pro296=
ENST00000409551.7:c.885C>A	ENSP00000386750.3:p.Pro295=
ENST00000464706.5:n.312C>A
ENST00000555548.1:n.119C>A
NM_001127366.2:c.885C>A	NP_001120838.1:p.Pro295=
NM_181457.3:c.888C>A	NP_852122.1:p.Pro296=
NM_181458.3:c.888C>A	NP_852123.1:p.Pro296=
NM_181459.3:c.888C>A	NP_852124.1:p.Pro296=
NM_181460.3:c.888C>A	NP_852125.1:p.Pro296=
NM_181461.3:c.888C>A	NP_852126.1:p.Pro296=
XM_011511278.1:c.1032C>A	XP_011509580.1:p.Pro344=
XM_011511279.1:c.324C>A	XP_011509581.1:p.Pro108=
NM_001127366.3:c.885C>A	NP_001120838.1:p.Pro295=
NM_181457.4:c.888C>A	NP_852122.1:p.Pro296=
NM_181458.4:c.888C>A MANE Select	NP_852123.1:p.Pro296=
NM_181459.4:c.888C>A	NP_852124.1:p.Pro296=
NM_181460.4:c.888C>A	NP_852125.1:p.Pro296=
NM_181461.4:c.888C>A	NP_852126.1:p.Pro296=