Canonical Allele Identifier: CA351116331
Community Standard Title: NM_181458.4(PAX3):c.994C>T (p.Gln332Ter)
Gene: PAX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222220319G>A , CM000664.2:g.222220319G>A GRCh38
NC_000002.11:g.223085038G>A , CM000664.1:g.223085038G>A GRCh37
NC_000002.10:g.222793282G>A NCBI36
NG_011632.1:g.83663C>T

Transcript Alleles

HGVS Amino-acid Change
NM_181458.4:c.994C>T MANE Select NP_852123.1:p.Gln332Ter
ENST00000392070.7:c.994C>T MANE Select ENSP00000375922.3:p.Gln332Ter
NM_001127366.2:c.991C>T NP_001120838.1:p.Gln331Ter
NM_001127366.3:c.991C>T NP_001120838.1:p.Gln331Ter
NM_181457.3:c.994C>T NP_852122.1:p.Gln332Ter
NM_181457.4:c.994C>T NP_852122.1:p.Gln332Ter
NM_181458.3:c.994C>T NP_852123.1:p.Gln332Ter
NM_181459.3:c.994C>T NP_852124.1:p.Gln332Ter
NM_181459.4:c.994C>T NP_852124.1:p.Gln332Ter
NM_181460.3:c.994C>T NP_852125.1:p.Gln332Ter
NM_181460.4:c.994C>T NP_852125.1:p.Gln332Ter
NM_181461.3:c.994C>T NP_852126.1:p.Gln332Ter
NM_181461.4:c.994C>T NP_852126.1:p.Gln332Ter
ENST00000336840.10:c.994C>T ENSP00000338767.5:p.Gln332Ter
ENST00000336840.11:c.994C>T ENSP00000338767.5:p.Gln332Ter
ENST00000344493.8:c.994C>T ENSP00000342092.4:p.Gln332Ter
ENST00000344493.9:c.994C>T ENSP00000342092.4:p.Gln332Ter
ENST00000350526.8:c.994C>T ENSP00000343052.4:p.Gln332Ter
ENST00000350526.9:c.994C>T ENSP00000343052.4:p.Gln332Ter
ENST00000392069.6:c.994C>T ENSP00000375921.2:p.Gln332Ter
ENST00000392070.6:c.994C>T ENSP00000375922.2:p.Gln332Ter
ENST00000409551.7:c.991C>T ENSP00000386750.3:p.Gln331Ter
ENST00000464706.5:n.418C>T
ENST00000464706.6:n.432C>T
ENST00000555548.1:n.225C>T
ENST00000644699.1:n.320C>T
ENST00000644937.1:n.266C>T
ENST00000646154.1:n.808C>T
XM_011511278.1:c.1138C>T XP_011509580.1:p.Gln380Ter
XM_011511279.1:c.430C>T XP_011509581.1:p.Gln144Ter
XR_001739903.1:n.240-77G>A