Canonical Allele Identifier: CA519892936

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14890151T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778217T>C , CM000686.2:g.12778217T>C	GRCh38
NC_000024.9:g.14890151T>C , CM000686.1:g.14890151T>C	GRCh37
NC_000024.8:g.13399545T>C	NCBI36
NG_008311.1:g.81992T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2838T>C	ENSP00000498372.1:p.Asp946=
ENST00000338981.7:c.2838T>C MANE Select	ENSP00000342812.3:p.Asp946=
ENST00000426564.6:n.2850T>C
NM_004654.3:c.2838T>C	NP_004645.2:p.Asp946=
XM_011531469.1:c.2838T>C	XP_011529771.1:p.Asp946=
XM_011531470.1:c.2604T>C	XP_011529772.1:p.Asp868=
XM_017030078.2:c.2853T>C	XP_016885567.1:p.Asp951=
NM_004654.4:c.2838T>C MANE Select	NP_004645.2:p.Asp946=