Canonical Allele Identifier: CA412763184
Gene: USP9X HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41136907C>T , CM000685.2:g.41136907C>T GRCh38
NC_000023.10:g.40996160C>T , CM000685.1:g.40996160C>T GRCh37
NC_000023.9:g.40881104C>T NCBI36
NG_012547.1:g.56273C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703986.1:c.539C>T ENSP00000515603.1:p.Pro180Leu
ENST00000703987.1:c.539C>T ENSP00000515604.1:p.Pro180Leu
ENST00000704649.1:c.539C>T ENSP00000515974.1:p.Pro180Leu
ENST00000704650.1:c.539C>T ENSP00000515975.1:p.Pro180Leu
ENST00000704651.1:c.539C>T ENSP00000515976.1:p.Pro180Leu
ENST00000324545.9:c.539C>T ENSP00000316357.6:p.Pro180Leu
ENST00000378308.7:c.539C>T MANE Select ENSP00000367558.2:p.Pro180Leu
ENST00000324545.8:c.539C>T ENSP00000316357.6:p.Pro180Leu
ENST00000378308.6:c.539C>T ENSP00000367558.2:p.Pro180Leu
NM_001039590.2:c.539C>T NP_001034679.2:p.Pro180Leu
NM_001039591.2:c.539C>T NP_001034680.2:p.Pro180Leu
XM_005272675.3:c.539C>T XP_005272732.1:p.Pro180Leu
XM_005272676.3:c.539C>T XP_005272733.1:p.Pro180Leu
XM_005272675.4:c.539C>T XP_005272732.1:p.Pro180Leu
XM_005272676.4:c.539C>T XP_005272733.1:p.Pro180Leu
NM_001039591.3:c.539C>T MANE Select NP_001034680.2:p.Pro180Leu
NM_001039590.3:c.539C>T NP_001034679.2:p.Pro180Leu