Canonical Allele Identifier: CA414986480

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14969554T>G (hg19) ; chrY:g.12857629T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12857629T>G , CM000686.2:g.12857629T>G	GRCh38
NC_000024.9:g.14969554T>G , CM000686.1:g.14969554T>G	GRCh37
NC_000024.8:g.13478948T>G	NCBI36
NG_008311.1:g.161395T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.7498T>G	ENSP00000498372.1:p.Tyr2500Asp
ENST00000338981.7:c.7498T>G MANE Select	ENSP00000342812.3:p.Tyr2500Asp
ENST00000426564.6:n.7525T>G
ENST00000453031.1:c.543T>G
ENST00000471409.1:n.817T>G
NM_004654.3:c.7498T>G	NP_004645.2:p.Tyr2500Asp
XM_011531469.1:c.7498T>G	XP_011529771.1:p.Tyr2500Asp
XM_011531470.1:c.7264T>G	XP_011529772.1:p.Tyr2422Asp
XM_017030078.2:c.7513T>G	XP_016885567.1:p.Tyr2505Asp
NM_004654.4:c.7498T>G MANE Select	NP_004645.2:p.Tyr2500Asp