Canonical Allele Identifier: CA414981972

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14838707C>T (hg19) ; chrY:g.12726774C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12726774C>T , CM000686.2:g.12726774C>T	GRCh38
NC_000024.9:g.14838707C>T , CM000686.1:g.14838707C>T	GRCh37
NC_000024.8:g.13348101C>T	NCBI36
NG_008311.1:g.30548C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.638C>T	ENSP00000498372.1:p.Ser213Leu
ENST00000338981.7:c.638C>T MANE Select	ENSP00000342812.3:p.Ser213Leu
ENST00000426564.6:n.650C>T
NM_004654.3:c.638C>T	NP_004645.2:p.Ser213Leu
XM_011531469.1:c.638C>T	XP_011529771.1:p.Ser213Leu
XM_011531470.1:c.404C>T	XP_011529772.1:p.Ser135Leu
XM_017030078.2:c.638C>T	XP_016885567.1:p.Ser213Leu
NM_004654.4:c.638C>T MANE Select	NP_004645.2:p.Ser213Leu