Canonical Allele Identifier: CA414986502

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14969557C>A (hg19) ; chrY:g.12857632C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12857632C>A , CM000686.2:g.12857632C>A	GRCh38
NC_000024.9:g.14969557C>A , CM000686.1:g.14969557C>A	GRCh37
NC_000024.8:g.13478951C>A	NCBI36
NG_008311.1:g.161398C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.7501C>A	ENSP00000498372.1:p.Pro2501Thr
ENST00000338981.7:c.7501C>A MANE Select	ENSP00000342812.3:p.Pro2501Thr
ENST00000426564.6:n.7528C>A
ENST00000453031.1:c.546C>A
ENST00000471409.1:n.820C>A
NM_004654.3:c.7501C>A	NP_004645.2:p.Pro2501Thr
XM_011531469.1:c.7501C>A	XP_011529771.1:p.Pro2501Thr
XM_011531470.1:c.7267C>A	XP_011529772.1:p.Pro2423Thr
XM_017030078.2:c.7516C>A	XP_016885567.1:p.Pro2506Thr
NM_004654.4:c.7501C>A MANE Select	NP_004645.2:p.Pro2501Thr