Canonical Allele Identifier: CA351115855

Gene: PAX3

Linked Data

• MyVariant Identifiers: chr2:g.223066871A>C (hg19) ; chr2:g.222202152A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222202152A>C , CM000664.2:g.222202152A>C	GRCh38
NC_000002.11:g.223066871A>C , CM000664.1:g.223066871A>C	GRCh37
NC_000002.10:g.222775115A>C	NCBI36
NG_011632.1:g.101830T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.1174-710T>G	ENSP00000338767.5:n.1174-710T>G
ENST00000344493.9:c.1174-710T>G	ENSP00000342092.4:n.1174-710T>G
ENST00000350526.9:c.1212T>G	ENSP00000343052.4:p.His404Gln
ENST00000392070.7:c.1212T>G MANE Select	ENSP00000375922.3:p.His404Gln
ENST00000464706.6:n.650T>G
ENST00000644699.1:n.538T>G
ENST00000646154.1:n.1026T>G
ENST00000336840.10:c.1174-710T>G	ENSP00000338767.5:n.1174-710T>G
ENST00000344493.8:c.1174-710T>G	ENSP00000342092.4:n.1174-710T>G
ENST00000350526.8:c.1212T>G	ENSP00000343052.4:p.His404Gln
ENST00000392069.6:c.1212T>G	ENSP00000375921.2:p.His404Gln
ENST00000392070.6:c.1212T>G	ENSP00000375922.2:p.His404Gln
ENST00000409551.7:c.1209T>G	ENSP00000386750.3:p.His403Gln
ENST00000464706.5:n.636T>G
ENST00000555548.1:n.443T>G
NM_001127366.2:c.1209T>G	NP_001120838.1:p.His403Gln
NM_181457.3:c.1212T>G	NP_852122.1:p.His404Gln
NM_181458.3:c.1212T>G	NP_852123.1:p.His404Gln
NM_181459.3:c.1212T>G	NP_852124.1:p.His404Gln
NM_181460.3:c.1174-710T>G	NP_852125.1:n.1174-710T>G
NM_181461.3:c.1174-710T>G	NP_852126.1:n.1174-710T>G
XM_011511278.1:c.1356T>G	XP_011509580.1:p.His452Gln
XM_011511279.1:c.648T>G	XP_011509581.1:p.His216Gln
NM_001127366.3:c.1209T>G	NP_001120838.1:p.His403Gln
NM_181457.4:c.1212T>G	NP_852122.1:p.His404Gln
NM_181458.4:c.1212T>G MANE Select	NP_852123.1:p.His404Gln
NM_181459.4:c.1212T>G	NP_852124.1:p.His404Gln
NM_181460.4:c.1174-710T>G	NP_852125.1:n.1174-710T>G
NM_181461.4:c.1174-710T>G	NP_852126.1:n.1174-710T>G