Canonical Allele Identifier: CA414981957

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14838700C>G (hg19) ; chrY:g.12726767C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12726767C>G , CM000686.2:g.12726767C>G	GRCh38
NC_000024.9:g.14838700C>G , CM000686.1:g.14838700C>G	GRCh37
NC_000024.8:g.13348094C>G	NCBI36
NG_008311.1:g.30541C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.631C>G	ENSP00000498372.1:p.Arg211Gly
ENST00000338981.7:c.631C>G MANE Select	ENSP00000342812.3:p.Arg211Gly
ENST00000426564.6:n.643C>G
NM_004654.3:c.631C>G	NP_004645.2:p.Arg211Gly
XM_011531469.1:c.631C>G	XP_011529771.1:p.Arg211Gly
XM_011531470.1:c.397C>G	XP_011529772.1:p.Arg133Gly
XM_017030078.2:c.631C>G	XP_016885567.1:p.Arg211Gly
NM_004654.4:c.631C>G MANE Select	NP_004645.2:p.Arg211Gly