Canonical Allele Identifier: CA414983427
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790414A>T , CM000686.2:g.12790414A>T GRCh38
NC_000024.9:g.14902347A>T , CM000686.1:g.14902347A>T GRCh37
NC_000024.8:g.13411741A>T NCBI36
NG_008311.1:g.94188A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.3569A>T ENSP00000498372.1:p.Gln1190Leu
ENST00000338981.7:c.3569A>T MANE Select ENSP00000342812.3:p.Gln1190Leu
ENST00000426564.6:n.3581A>T
NM_004654.3:c.3569A>T NP_004645.2:p.Gln1190Leu
XM_011531469.1:c.3569A>T XP_011529771.1:p.Gln1190Leu
XM_011531470.1:c.3335A>T XP_011529772.1:p.Gln1112Leu
XM_017030078.2:c.3584A>T XP_016885567.1:p.Gln1195Leu
NM_004654.4:c.3569A>T MANE Select NP_004645.2:p.Gln1190Leu