Canonical Allele Identifier: CA519892163

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14890061A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778127A>T , CM000686.2:g.12778127A>T	GRCh38
NC_000024.9:g.14890061A>T , CM000686.1:g.14890061A>T	GRCh37
NC_000024.8:g.13399455A>T	NCBI36
NG_008311.1:g.81902A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2748A>T	ENSP00000498372.1:p.Val916=
ENST00000338981.7:c.2748A>T MANE Select	ENSP00000342812.3:p.Val916=
ENST00000426564.6:n.2760A>T
NM_004654.3:c.2748A>T	NP_004645.2:p.Val916=
XM_011531469.1:c.2748A>T	XP_011529771.1:p.Val916=
XM_011531470.1:c.2514A>T	XP_011529772.1:p.Val838=
XM_017030078.2:c.2763A>T	XP_016885567.1:p.Val921=
NM_004654.4:c.2748A>T MANE Select	NP_004645.2:p.Val916=