Canonical Allele Identifier: CA1330546588
Gene: PAX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222297215T= , CM000664.2:g.222297215T= GRCh38
NC_000002.11:g.223161934T= , CM000664.1:g.223161934T= GRCh37
NC_000002.10:g.222870178T= NCBI36
NG_011632.1:g.6767A=
NG_021186.1:g.4069T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258387.6:c.86-2A= ENSP00000258387.5:n.86-2A=
ENST00000336840.11:c.86-2A= ENSP00000338767.5:n.86-2A=
ENST00000344493.9:c.86-2A= ENSP00000342092.4:n.86-2A=
ENST00000350526.9:c.86-2A= ENSP00000343052.4:n.86-2A=
ENST00000392070.7:c.86-2A= MANE Select ENSP00000375922.3:n.86-2A=
ENST00000647467.1:n.467-2A=
ENST00000258387.5:c.86-2A= ENSP00000258387.5:n.86-2A=
ENST00000336840.10:c.86-2A= ENSP00000338767.5:n.86-2A=
ENST00000344493.8:c.86-2A= ENSP00000342092.4:n.86-2A=
ENST00000350526.8:c.86-2A= ENSP00000343052.4:n.86-2A=
ENST00000392069.6:c.86-2A= ENSP00000375921.2:n.86-2A=
ENST00000392070.6:c.86-2A= ENSP00000375922.2:n.86-2A=
ENST00000409551.7:c.86-2A= ENSP00000386750.3:n.86-2A=
ENST00000409828.7:c.86-2A= ENSP00000386817.3:n.86-2A=
NM_000438.5:c.86-2A= NP_000429.2:n.86-2A=
NM_001127366.2:c.86-2A= NP_001120838.1:n.86-2A=
NM_013942.4:c.86-2A= NP_039230.1:n.86-2A=
NM_181457.3:c.86-2A= NP_852122.1:n.86-2A=
NM_181458.3:c.86-2A= NP_852123.1:n.86-2A=
NM_181459.3:c.86-2A= NP_852124.1:n.86-2A=
NM_181460.3:c.86-2A= NP_852125.1:n.86-2A=
NM_181461.3:c.86-2A= NP_852126.1:n.86-2A=
XM_011511278.1:c.230-2A= XP_011509580.1:n.230-2A=
XM_011511280.1:c.230-2A= XP_011509582.1:n.230-2A=
XM_011511281.1:c.230-2A= XP_011509583.1:n.230-2A=
NM_000438.6:c.86-2A= NP_000429.2:n.86-2A=
NM_001127366.3:c.86-2A= NP_001120838.1:n.86-2A=
NM_013942.5:c.86-2A= NP_039230.1:n.86-2A=
NM_181457.4:c.86-2A= NP_852122.1:n.86-2A=
NM_181458.4:c.86-2A= MANE Select NP_852123.1:n.86-2A=
NM_181459.4:c.86-2A= NP_852124.1:n.86-2A=
NM_181460.4:c.86-2A= NP_852125.1:n.86-2A=
NM_181461.4:c.86-2A= NP_852126.1:n.86-2A=