Canonical Allele Identifier: CA415007739
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778069G>T , CM000686.2:g.12778069G>T GRCh38
NC_000024.9:g.14890003G>T , CM000686.1:g.14890003G>T GRCh37
NC_000024.8:g.13399397G>T NCBI36
NG_008311.1:g.81844G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2690G>T ENSP00000498372.1:p.Gly897Val
ENST00000338981.7:c.2690G>T MANE Select ENSP00000342812.3:p.Gly897Val
ENST00000426564.6:n.2702G>T
NM_004654.3:c.2690G>T NP_004645.2:p.Gly897Val
XM_011531469.1:c.2690G>T XP_011529771.1:p.Gly897Val
XM_011531470.1:c.2456G>T XP_011529772.1:p.Gly819Val
XM_017030078.2:c.2705G>T XP_016885567.1:p.Gly902Val
NM_004654.4:c.2690G>T MANE Select NP_004645.2:p.Gly897Val