Canonical Allele Identifier: CA431575506

Gene: PAX3

Linked Data

• MyVariant Identifiers: chr2:g.223085990T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222221271T>G , CM000664.2:g.222221271T>G	GRCh38
NC_000002.11:g.223085990T>G , CM000664.1:g.223085990T>G	GRCh37
NC_000002.10:g.222794234T>G	NCBI36
NG_011632.1:g.82711A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.909A>C	ENSP00000338767.5:p.Pro303=
ENST00000344493.9:c.909A>C	ENSP00000342092.4:p.Pro303=
ENST00000350526.9:c.909A>C	ENSP00000343052.4:p.Pro303=
ENST00000392070.7:c.909A>C MANE Select	ENSP00000375922.3:p.Pro303=
ENST00000464706.6:n.347A>C
ENST00000644699.1:n.235A>C
ENST00000644937.1:n.181A>C
ENST00000646154.1:n.723A>C
ENST00000336840.10:c.909A>C	ENSP00000338767.5:p.Pro303=
ENST00000344493.8:c.909A>C	ENSP00000342092.4:p.Pro303=
ENST00000350526.8:c.909A>C	ENSP00000343052.4:p.Pro303=
ENST00000392069.6:c.909A>C	ENSP00000375921.2:p.Pro303=
ENST00000392070.6:c.909A>C	ENSP00000375922.2:p.Pro303=
ENST00000409551.7:c.906A>C	ENSP00000386750.3:p.Pro302=
ENST00000464706.5:n.333A>C
ENST00000555548.1:n.140A>C
NM_001127366.2:c.906A>C	NP_001120838.1:p.Pro302=
NM_181457.3:c.909A>C	NP_852122.1:p.Pro303=
NM_181458.3:c.909A>C	NP_852123.1:p.Pro303=
NM_181459.3:c.909A>C	NP_852124.1:p.Pro303=
NM_181460.3:c.909A>C	NP_852125.1:p.Pro303=
NM_181461.3:c.909A>C	NP_852126.1:p.Pro303=
XM_011511278.1:c.1053A>C	XP_011509580.1:p.Pro351=
XM_011511279.1:c.345A>C	XP_011509581.1:p.Pro115=
NM_001127366.3:c.906A>C	NP_001120838.1:p.Pro302=
NM_181457.4:c.909A>C	NP_852122.1:p.Pro303=
NM_181458.4:c.909A>C MANE Select	NP_852123.1:p.Pro303=
NM_181459.4:c.909A>C	NP_852124.1:p.Pro303=
NM_181460.4:c.909A>C	NP_852125.1:p.Pro303=
NM_181461.4:c.909A>C	NP_852126.1:p.Pro303=