Canonical Allele Identifier: CA431575487

Gene: PAX3

Linked Data

• MyVariant Identifiers: chr2:g.223085960C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222221241C>T , CM000664.2:g.222221241C>T	GRCh38
NC_000002.11:g.223085960C>T , CM000664.1:g.223085960C>T	GRCh37
NC_000002.10:g.222794204C>T	NCBI36
NG_011632.1:g.82741G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.939G>A	ENSP00000338767.5:p.Gln313=
ENST00000344493.9:c.939G>A	ENSP00000342092.4:p.Gln313=
ENST00000350526.9:c.939G>A	ENSP00000343052.4:p.Gln313=
ENST00000392070.7:c.939G>A MANE Select	ENSP00000375922.3:p.Gln313=
ENST00000464706.6:n.377G>A
ENST00000644699.1:n.265G>A
ENST00000644937.1:n.211G>A
ENST00000646154.1:n.753G>A
ENST00000336840.10:c.939G>A	ENSP00000338767.5:p.Gln313=
ENST00000344493.8:c.939G>A	ENSP00000342092.4:p.Gln313=
ENST00000350526.8:c.939G>A	ENSP00000343052.4:p.Gln313=
ENST00000392069.6:c.939G>A	ENSP00000375921.2:p.Gln313=
ENST00000392070.6:c.939G>A	ENSP00000375922.2:p.Gln313=
ENST00000409551.7:c.936G>A	ENSP00000386750.3:p.Gln312=
ENST00000464706.5:n.363G>A
ENST00000555548.1:n.170G>A
NM_001127366.2:c.936G>A	NP_001120838.1:p.Gln312=
NM_181457.3:c.939G>A	NP_852122.1:p.Gln313=
NM_181458.3:c.939G>A	NP_852123.1:p.Gln313=
NM_181459.3:c.939G>A	NP_852124.1:p.Gln313=
NM_181460.3:c.939G>A	NP_852125.1:p.Gln313=
NM_181461.3:c.939G>A	NP_852126.1:p.Gln313=
XM_011511278.1:c.1083G>A	XP_011509580.1:p.Gln361=
XM_011511279.1:c.375G>A	XP_011509581.1:p.Gln125=
NM_001127366.3:c.936G>A	NP_001120838.1:p.Gln312=
NM_181457.4:c.939G>A	NP_852122.1:p.Gln313=
NM_181458.4:c.939G>A MANE Select	NP_852123.1:p.Gln313=
NM_181459.4:c.939G>A	NP_852124.1:p.Gln313=
NM_181460.4:c.939G>A	NP_852125.1:p.Gln313=
NM_181461.4:c.939G>A	NP_852126.1:p.Gln313=