Canonical Allele Identifier: CA519856367

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14832542C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12720609C>T , CM000686.2:g.12720609C>T	GRCh38
NC_000024.9:g.14832542C>T , CM000686.1:g.14832542C>T	GRCh37
NC_000024.8:g.13341936C>T	NCBI36
NG_008311.1:g.24383C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.117C>T	ENSP00000498372.1:p.Ser39=
ENST00000338981.7:c.117C>T MANE Select	ENSP00000342812.3:p.Ser39=
ENST00000426564.6:n.129C>T
ENST00000493168.1:n.193C>T
NM_004654.3:c.117C>T	NP_004645.2:p.Ser39=
XM_011531469.1:c.117C>T	XP_011529771.1:p.Ser39=
XM_011531470.1:c.-118C>T	XP_011529772.1:n.-118C>T
XM_017030078.2:c.117C>T	XP_016885567.1:p.Ser39=
NM_004654.4:c.117C>T MANE Select	NP_004645.2:p.Ser39=