Canonical Allele Identifier: CA519901484

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14945632T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833706T>C , CM000686.2:g.12833706T>C	GRCh38
NC_000024.9:g.14945632T>C , CM000686.1:g.14945632T>C	GRCh37
NC_000024.8:g.13455026T>C	NCBI36
NG_008311.1:g.137473T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.5040T>C	ENSP00000498372.1:p.Val1680=
ENST00000338981.7:c.5040T>C MANE Select	ENSP00000342812.3:p.Val1680=
ENST00000426564.6:n.5052T>C
NM_004654.3:c.5040T>C	NP_004645.2:p.Val1680=
XM_011531469.1:c.5040T>C	XP_011529771.1:p.Val1680=
XM_011531470.1:c.4806T>C	XP_011529772.1:p.Val1602=
XM_017030078.2:c.5055T>C	XP_016885567.1:p.Val1685=
NM_004654.4:c.5040T>C MANE Select	NP_004645.2:p.Val1680=