Canonical Allele Identifier: CA414986384

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14969546C>A (hg19) ; chrY:g.12857621C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12857621C>A , CM000686.2:g.12857621C>A	GRCh38
NC_000024.9:g.14969546C>A , CM000686.1:g.14969546C>A	GRCh37
NC_000024.8:g.13478940C>A	NCBI36
NG_008311.1:g.161387C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.7490C>A	ENSP00000498372.1:p.Ala2497Asp
ENST00000338981.7:c.7490C>A MANE Select	ENSP00000342812.3:p.Ala2497Asp
ENST00000426564.6:n.7517C>A
ENST00000453031.1:c.535C>A
ENST00000471409.1:n.809C>A
NM_004654.3:c.7490C>A	NP_004645.2:p.Ala2497Asp
XM_011531469.1:c.7490C>A	XP_011529771.1:p.Ala2497Asp
XM_011531470.1:c.7256C>A	XP_011529772.1:p.Ala2419Asp
XM_017030078.2:c.7505C>A	XP_016885567.1:p.Ala2502Asp
NM_004654.4:c.7490C>A MANE Select	NP_004645.2:p.Ala2497Asp