Canonical Allele Identifier: CA431575835
Gene: PAX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.223160317G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222295598G>T , CM000664.2:g.222295598G>T GRCh38
NC_000002.11:g.223160317G>T , CM000664.1:g.223160317G>T GRCh37
NC_000002.10:g.222868561G>T NCBI36
NG_011632.1:g.8384C>A
NG_021186.1:g.2452G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258387.6:c.381C>A ENSP00000258387.5:p.Gly127=
ENST00000336840.11:c.381C>A ENSP00000338767.5:p.Gly127=
ENST00000344493.9:c.381C>A ENSP00000342092.4:p.Gly127=
ENST00000350526.9:c.381C>A ENSP00000343052.4:p.Gly127=
ENST00000392070.7:c.381C>A MANE Select ENSP00000375922.3:p.Gly127=
ENST00000647467.1:n.762C>A
ENST00000258387.5:c.381C>A ENSP00000258387.5:p.Gly127=
ENST00000336840.10:c.381C>A ENSP00000338767.5:p.Gly127=
ENST00000344493.8:c.381C>A ENSP00000342092.4:p.Gly127=
ENST00000350526.8:c.381C>A ENSP00000343052.4:p.Gly127=
ENST00000392069.6:c.381C>A ENSP00000375921.2:p.Gly127=
ENST00000392070.6:c.381C>A ENSP00000375922.2:p.Gly127=
ENST00000409551.7:c.378C>A ENSP00000386750.3:p.Gly126=
ENST00000409828.7:c.381C>A ENSP00000386817.3:p.Gly127=
NM_000438.5:c.381C>A NP_000429.2:p.Gly127=
NM_001127366.2:c.378C>A NP_001120838.1:p.Gly126=
NM_013942.4:c.381C>A NP_039230.1:p.Gly127=
NM_181457.3:c.381C>A NP_852122.1:p.Gly127=
NM_181458.3:c.381C>A NP_852123.1:p.Gly127=
NM_181459.3:c.381C>A NP_852124.1:p.Gly127=
NM_181460.3:c.381C>A NP_852125.1:p.Gly127=
NM_181461.3:c.381C>A NP_852126.1:p.Gly127=
XM_011511278.1:c.525C>A XP_011509580.1:p.Gly175=
XM_011511280.1:c.525C>A XP_011509582.1:p.Gly175=
XM_011511281.1:c.525C>A XP_011509583.1:p.Gly175=
NM_000438.6:c.381C>A NP_000429.2:p.Gly127=
NM_001127366.3:c.378C>A NP_001120838.1:p.Gly126=
NM_013942.5:c.381C>A NP_039230.1:p.Gly127=
NM_181457.4:c.381C>A NP_852122.1:p.Gly127=
NM_181458.4:c.381C>A MANE Select NP_852123.1:p.Gly127=
NM_181459.4:c.381C>A NP_852124.1:p.Gly127=
NM_181460.4:c.381C>A NP_852125.1:p.Gly127=
NM_181461.4:c.381C>A NP_852126.1:p.Gly127=