Canonical Allele Identifier: CA414998880
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12833749T>G , CM000686.2:g.12833749T>G GRCh38
NC_000024.9:g.14945675T>G , CM000686.1:g.14945675T>G GRCh37
NC_000024.8:g.13455069T>G NCBI36
NG_008311.1:g.137516T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.5083T>G ENSP00000498372.1:p.Leu1695Val
ENST00000338981.7:c.5083T>G MANE Select ENSP00000342812.3:p.Leu1695Val
ENST00000426564.6:n.5095T>G
NM_004654.3:c.5083T>G NP_004645.2:p.Leu1695Val
XM_011531469.1:c.5083T>G XP_011529771.1:p.Leu1695Val
XM_011531470.1:c.4849T>G XP_011529772.1:p.Leu1617Val
XM_017030078.2:c.5098T>G XP_016885567.1:p.Leu1700Val
NM_004654.4:c.5083T>G MANE Select NP_004645.2:p.Leu1695Val