Canonical Allele Identifier: CA519875029

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14969571C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12857646C>G , CM000686.2:g.12857646C>G	GRCh38
NC_000024.9:g.14969571C>G , CM000686.1:g.14969571C>G	GRCh37
NC_000024.8:g.13478965C>G	NCBI36
NG_008311.1:g.161412C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.7515C>G	ENSP00000498372.1:p.Ala2505=
ENST00000338981.7:c.7515C>G MANE Select	ENSP00000342812.3:p.Ala2505=
ENST00000426564.6:n.7542C>G
ENST00000453031.1:c.560C>G
ENST00000471409.1:n.834C>G
NM_004654.3:c.7515C>G	NP_004645.2:p.Ala2505=
XM_011531469.1:c.7515C>G	XP_011529771.1:p.Ala2505=
XM_011531470.1:c.7281C>G	XP_011529772.1:p.Ala2427=
XM_017030078.2:c.7530C>G	XP_016885567.1:p.Ala2510=
NM_004654.4:c.7515C>G MANE Select	NP_004645.2:p.Ala2505=