Canonical Allele Identifier: CA414986784

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14969586G>T (hg19) ; chrY:g.12857661G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12857661G>T , CM000686.2:g.12857661G>T	GRCh38
NC_000024.9:g.14969586G>T , CM000686.1:g.14969586G>T	GRCh37
NC_000024.8:g.13478980G>T	NCBI36
NG_008311.1:g.161427G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.7530G>T	ENSP00000498372.1:p.Gln2510His
ENST00000338981.7:c.7530G>T MANE Select	ENSP00000342812.3:p.Gln2510His
ENST00000426564.6:n.7557G>T
ENST00000453031.1:c.575G>T
ENST00000471409.1:n.849G>T
NM_004654.3:c.7530G>T	NP_004645.2:p.Gln2510His
XM_011531469.1:c.7530G>T	XP_011529771.1:p.Gln2510His
XM_011531470.1:c.7296G>T	XP_011529772.1:p.Gln2432His
XM_017030078.2:c.7545G>T	XP_016885567.1:p.Gln2515His
NM_004654.4:c.7530G>T MANE Select	NP_004645.2:p.Gln2510His