Canonical Allele Identifier: CA415007505

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14958307T>G (hg19) ; chrY:g.12846382T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12846382T>G , CM000686.2:g.12846382T>G	GRCh38
NC_000024.9:g.14958307T>G , CM000686.1:g.14958307T>G	GRCh37
NC_000024.8:g.13467701T>G	NCBI36
NG_008311.1:g.150148T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.6618T>G	ENSP00000498372.1:p.Phe2206Leu
ENST00000338981.7:c.6618T>G MANE Select	ENSP00000342812.3:p.Phe2206Leu
ENST00000426564.6:n.6645T>G
NM_004654.3:c.6618T>G	NP_004645.2:p.Phe2206Leu
XM_011531469.1:c.6618T>G	XP_011529771.1:p.Phe2206Leu
XM_011531470.1:c.6384T>G	XP_011529772.1:p.Phe2128Leu
XM_017030078.2:c.6633T>G	XP_016885567.1:p.Phe2211Leu
NM_004654.4:c.6618T>G MANE Select	NP_004645.2:p.Phe2206Leu