Canonical Allele Identifier: CA415007793

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14958357A>C (hg19) ; chrY:g.12846432A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12846432A>C , CM000686.2:g.12846432A>C	GRCh38
NC_000024.9:g.14958357A>C , CM000686.1:g.14958357A>C	GRCh37
NC_000024.8:g.13467751A>C	NCBI36
NG_008311.1:g.150198A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.6668A>C	ENSP00000498372.1:p.Tyr2223Ser
ENST00000338981.7:c.6668A>C MANE Select	ENSP00000342812.3:p.Tyr2223Ser
ENST00000426564.6:n.6695A>C
NM_004654.3:c.6668A>C	NP_004645.2:p.Tyr2223Ser
XM_011531469.1:c.6668A>C	XP_011529771.1:p.Tyr2223Ser
XM_011531470.1:c.6434A>C	XP_011529772.1:p.Tyr2145Ser
XM_017030078.2:c.6683A>C	XP_016885567.1:p.Tyr2228Ser
NM_004654.4:c.6668A>C MANE Select	NP_004645.2:p.Tyr2223Ser