Canonical Allele Identifier: CA414984668

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14847632A>T (hg19) ; chrY:g.12735698A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12735698A>T , CM000686.2:g.12735698A>T	GRCh38
NC_000024.9:g.14847632A>T , CM000686.1:g.14847632A>T	GRCh37
NC_000024.8:g.13357026A>T	NCBI36
NG_008311.1:g.39473A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.744A>T	ENSP00000498372.1:p.Leu248Phe
ENST00000338981.7:c.744A>T MANE Select	ENSP00000342812.3:p.Leu248Phe
ENST00000426564.6:n.756A>T
NM_004654.3:c.744A>T	NP_004645.2:p.Leu248Phe
XM_011531469.1:c.744A>T	XP_011529771.1:p.Leu248Phe
XM_011531470.1:c.510A>T	XP_011529772.1:p.Leu170Phe
XM_017030078.2:c.744A>T	XP_016885567.1:p.Leu248Phe
NM_004654.4:c.744A>T MANE Select	NP_004645.2:p.Leu248Phe