Canonical Allele Identifier: CA1330502824

Gene: PAX3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222202128G= , CM000664.2:g.222202128G=	GRCh38
NC_000002.11:g.223066847G= , CM000664.1:g.223066847G=	GRCh37
NC_000002.10:g.222775091G=	NCBI36
NG_011632.1:g.101854C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.1174-686C=	ENSP00000338767.5:n.1174-686C=
ENST00000344493.9:c.1174-686C=	ENSP00000342092.4:n.1174-686C=
ENST00000350526.9:c.1236C=	ENSP00000343052.4:p.Leu412=
ENST00000392070.7:c.1236C= MANE Select	ENSP00000375922.3:p.Leu412=
ENST00000464706.6:n.674C=
ENST00000644699.1:n.562C=
ENST00000646154.1:n.1050C=
ENST00000336840.10:c.1174-686C=	ENSP00000338767.5:n.1174-686C=
ENST00000344493.8:c.1174-686C=	ENSP00000342092.4:n.1174-686C=
ENST00000350526.8:c.1236C=	ENSP00000343052.4:p.Leu412=
ENST00000392069.6:c.1236C=	ENSP00000375921.2:p.Leu412=
ENST00000392070.6:c.1236C=	ENSP00000375922.2:p.Leu412=
ENST00000409551.7:c.1233C=	ENSP00000386750.3:p.Leu411=
ENST00000464706.5:n.660C=
NM_001127366.2:c.1233C=	NP_001120838.1:p.Leu411=
NM_181457.3:c.1236C=	NP_852122.1:p.Leu412=
NM_181458.3:c.1236C=	NP_852123.1:p.Leu412=
NM_181459.3:c.1236C=	NP_852124.1:p.Leu412=
NM_181460.3:c.1174-686C=	NP_852125.1:n.1174-686C=
NM_181461.3:c.1174-686C=	NP_852126.1:n.1174-686C=
XM_011511278.1:c.1380C=	XP_011509580.1:p.Leu460=
XM_011511279.1:c.672C=	XP_011509581.1:p.Leu224=
NM_001127366.3:c.1233C=	NP_001120838.1:p.Leu411=
NM_181457.4:c.1236C=	NP_852122.1:p.Leu412=
NM_181458.4:c.1236C= MANE Select	NP_852123.1:p.Leu412=
NM_181459.4:c.1236C=	NP_852124.1:p.Leu412=
NM_181460.4:c.1174-686C=	NP_852125.1:n.1174-686C=
NM_181461.4:c.1174-686C=	NP_852126.1:n.1174-686C=