Canonical Allele Identifier: CA1330546473
Gene: PAX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.222296964_222296965delinsGC , CM000664.2:g.222296964_222296965delinsGC GRCh38
NC_000002.11:g.223161683_223161684delinsGC , CM000664.1:g.223161683_223161684delinsGC GRCh37
NC_000002.10:g.222869927_222869928delinsGC NCBI36
NG_011632.1:g.7017_7018delinsGC
NG_021186.1:g.3818_3819delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000258387.6:c.321+13_321+14delinsGC ENSP00000258387.5:n.321+13_321+14delinsGC
ENST00000336840.11:c.321+13_321+14delinsGC ENSP00000338767.5:n.321+13_321+14delinsGC
ENST00000344493.9:c.321+13_321+14delinsGC ENSP00000342092.4:n.321+13_321+14delinsGC
ENST00000350526.9:c.321+13_321+14delinsGC ENSP00000343052.4:n.321+13_321+14delinsGC
ENST00000392070.7:c.321+13_321+14delinsGC MANE Select ENSP00000375922.3:n.321+13_321+14delinsGC
ENST00000647467.1:n.702+13_702+14delinsGC
ENST00000258387.5:c.321+13_321+14delinsGC ENSP00000258387.5:n.321+13_321+14delinsGC
ENST00000336840.10:c.321+13_321+14delinsGC ENSP00000338767.5:n.321+13_321+14delinsGC
ENST00000344493.8:c.321+13_321+14delinsGC ENSP00000342092.4:n.321+13_321+14delinsGC
ENST00000350526.8:c.321+13_321+14delinsGC ENSP00000343052.4:n.321+13_321+14delinsGC
ENST00000392069.6:c.321+13_321+14delinsGC ENSP00000375921.2:n.321+13_321+14delinsGC
ENST00000392070.6:c.321+13_321+14delinsGC ENSP00000375922.2:n.321+13_321+14delinsGC
ENST00000409551.7:c.321+13_321+14delinsGC ENSP00000386750.3:n.321+13_321+14delinsGC
ENST00000409828.7:c.321+13_321+14delinsGC ENSP00000386817.3:n.321+13_321+14delinsGC
NM_000438.5:c.321+13_321+14delinsGC NP_000429.2:n.321+13_321+14delinsGC
NM_001127366.2:c.321+13_321+14delinsGC NP_001120838.1:n.321+13_321+14delinsGC
NM_013942.4:c.321+13_321+14delinsGC NP_039230.1:n.321+13_321+14delinsGC
NM_181457.3:c.321+13_321+14delinsGC NP_852122.1:n.321+13_321+14delinsGC
NM_181458.3:c.321+13_321+14delinsGC NP_852123.1:n.321+13_321+14delinsGC
NM_181459.3:c.321+13_321+14delinsGC NP_852124.1:n.321+13_321+14delinsGC
NM_181460.3:c.321+13_321+14delinsGC NP_852125.1:n.321+13_321+14delinsGC
NM_181461.3:c.321+13_321+14delinsGC NP_852126.1:n.321+13_321+14delinsGC
XM_011511278.1:c.465+13_465+14delinsGC XP_011509580.1:n.465+13_465+14delinsGC
XM_011511280.1:c.465+13_465+14delinsGC XP_011509582.1:n.465+13_465+14delinsGC
XM_011511281.1:c.465+13_465+14delinsGC XP_011509583.1:n.465+13_465+14delinsGC
NM_000438.6:c.321+13_321+14delinsGC NP_000429.2:n.321+13_321+14delinsGC
NM_001127366.3:c.321+13_321+14delinsGC NP_001120838.1:n.321+13_321+14delinsGC
NM_013942.5:c.321+13_321+14delinsGC NP_039230.1:n.321+13_321+14delinsGC
NM_181457.4:c.321+13_321+14delinsGC NP_852122.1:n.321+13_321+14delinsGC
NM_181458.4:c.321+13_321+14delinsGC MANE Select NP_852123.1:n.321+13_321+14delinsGC
NM_181459.4:c.321+13_321+14delinsGC NP_852124.1:n.321+13_321+14delinsGC
NM_181460.4:c.321+13_321+14delinsGC NP_852125.1:n.321+13_321+14delinsGC
NM_181461.4:c.321+13_321+14delinsGC NP_852126.1:n.321+13_321+14delinsGC