Canonical Allele Identifier: CA414986732

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14969579A>T (hg19) ; chrY:g.12857654A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12857654A>T , CM000686.2:g.12857654A>T	GRCh38
NC_000024.9:g.14969579A>T , CM000686.1:g.14969579A>T	GRCh37
NC_000024.8:g.13478973A>T	NCBI36
NG_008311.1:g.161420A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.7523A>T	ENSP00000498372.1:p.Tyr2508Phe
ENST00000338981.7:c.7523A>T MANE Select	ENSP00000342812.3:p.Tyr2508Phe
ENST00000426564.6:n.7550A>T
ENST00000453031.1:c.568A>T
ENST00000471409.1:n.842A>T
NM_004654.3:c.7523A>T	NP_004645.2:p.Tyr2508Phe
XM_011531469.1:c.7523A>T	XP_011529771.1:p.Tyr2508Phe
XM_011531470.1:c.7289A>T	XP_011529772.1:p.Tyr2430Phe
XM_017030078.2:c.7538A>T	XP_016885567.1:p.Tyr2513Phe
NM_004654.4:c.7523A>T MANE Select	NP_004645.2:p.Tyr2508Phe