Canonical Allele Identifier: CA414980728
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720698C>T , CM000686.2:g.12720698C>T GRCh38
NC_000024.9:g.14832631C>T , CM000686.1:g.14832631C>T GRCh37
NC_000024.8:g.13342025C>T NCBI36
NG_008311.1:g.24472C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.206C>T ENSP00000498372.1:p.Pro69Leu
ENST00000338981.7:c.206C>T MANE Select ENSP00000342812.3:p.Pro69Leu
ENST00000426564.6:n.218C>T
ENST00000493168.1:n.282C>T
NM_004654.3:c.206C>T NP_004645.2:p.Pro69Leu
XM_011531469.1:c.206C>T XP_011529771.1:p.Pro69Leu
XM_011531470.1:c.-29C>T XP_011529772.1:n.-29C>T
XM_017030078.2:c.206C>T XP_016885567.1:p.Pro69Leu
NM_004654.4:c.206C>T MANE Select NP_004645.2:p.Pro69Leu