Canonical Allele Identifier: CA412763104
Gene: USP9X HGNC NCBI

Linked Data

dbSNP Id: rs1191790572
gnomAD v2: X-40996148-T-C
gnomAD v4: X-41136895-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41136895T>C , CM000685.2:g.41136895T>C GRCh38
NC_000023.10:g.40996148T>C , CM000685.1:g.40996148T>C GRCh37
NC_000023.9:g.40881092T>C NCBI36
NG_012547.1:g.56261T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703986.1:c.527T>C ENSP00000515603.1:p.Met176Thr
ENST00000703987.1:c.527T>C ENSP00000515604.1:p.Met176Thr
ENST00000704649.1:c.527T>C ENSP00000515974.1:p.Met176Thr
ENST00000704650.1:c.527T>C ENSP00000515975.1:p.Met176Thr
ENST00000704651.1:c.527T>C ENSP00000515976.1:p.Met176Thr
ENST00000324545.9:c.527T>C ENSP00000316357.6:p.Met176Thr
ENST00000378308.7:c.527T>C MANE Select ENSP00000367558.2:p.Met176Thr
ENST00000324545.8:c.527T>C ENSP00000316357.6:p.Met176Thr
ENST00000378308.6:c.527T>C ENSP00000367558.2:p.Met176Thr
NM_001039590.2:c.527T>C NP_001034679.2:p.Met176Thr
NM_001039591.2:c.527T>C NP_001034680.2:p.Met176Thr
XM_005272675.3:c.527T>C XP_005272732.1:p.Met176Thr
XM_005272676.3:c.527T>C XP_005272733.1:p.Met176Thr
XM_005272675.4:c.527T>C XP_005272732.1:p.Met176Thr
XM_005272676.4:c.527T>C XP_005272733.1:p.Met176Thr
NM_001039591.3:c.527T>C MANE Select NP_001034680.2:p.Met176Thr
NM_001039590.3:c.527T>C NP_001034679.2:p.Met176Thr