Canonical Allele Identifier: CA414980523

Gene: USP9Y

Linked Data

• dbSNP Id: rs1288556749
• gnomAD v2: Y-14832541-C-T
• MyVariant Identifiers: chrY:g.14832541C>T (hg19) ; chrY:g.12720608C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12720608C>T , CM000686.2:g.12720608C>T	GRCh38
NC_000024.9:g.14832541C>T , CM000686.1:g.14832541C>T	GRCh37
NC_000024.8:g.13341935C>T	NCBI36
NG_008311.1:g.24382C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.116C>T	ENSP00000498372.1:p.Ser39Phe
ENST00000338981.7:c.116C>T MANE Select	ENSP00000342812.3:p.Ser39Phe
ENST00000426564.6:n.128C>T
ENST00000493168.1:n.192C>T
NM_004654.3:c.116C>T	NP_004645.2:p.Ser39Phe
XM_011531469.1:c.116C>T	XP_011529771.1:p.Ser39Phe
XM_011531470.1:c.-119C>T	XP_011529772.1:n.-119C>T
XM_017030078.2:c.116C>T	XP_016885567.1:p.Ser39Phe
NM_004654.4:c.116C>T MANE Select	NP_004645.2:p.Ser39Phe