Canonical Allele Identifier: CA414990121

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14922722T>C (hg19) ; chrY:g.12810787T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12810787T>C , CM000686.2:g.12810787T>C	GRCh38
NC_000024.9:g.14922722T>C , CM000686.1:g.14922722T>C	GRCh37
NC_000024.8:g.13432116T>C	NCBI36
NG_008311.1:g.114563T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.4208T>C	ENSP00000498372.1:p.Val1403Ala
ENST00000338981.7:c.4208T>C MANE Select	ENSP00000342812.3:p.Val1403Ala
ENST00000426564.6:n.4220T>C
NM_004654.3:c.4208T>C	NP_004645.2:p.Val1403Ala
XM_011531469.1:c.4208T>C	XP_011529771.1:p.Val1403Ala
XM_011531470.1:c.3974T>C	XP_011529772.1:p.Val1325Ala
XM_017030078.2:c.4223T>C	XP_016885567.1:p.Val1408Ala
NM_004654.4:c.4208T>C MANE Select	NP_004645.2:p.Val1403Ala