Canonical Allele Identifier: CA519901803

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14945713A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833787A>G , CM000686.2:g.12833787A>G	GRCh38
NC_000024.9:g.14945713A>G , CM000686.1:g.14945713A>G	GRCh37
NC_000024.8:g.13455107A>G	NCBI36
NG_008311.1:g.137554A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.5121A>G	ENSP00000498372.1:p.Gly1707=
ENST00000338981.7:c.5121A>G MANE Select	ENSP00000342812.3:p.Gly1707=
ENST00000426564.6:n.5133A>G
NM_004654.3:c.5121A>G	NP_004645.2:p.Gly1707=
XM_011531469.1:c.5121A>G	XP_011529771.1:p.Gly1707=
XM_011531470.1:c.4887A>G	XP_011529772.1:p.Gly1629=
XM_017030078.2:c.5136A>G	XP_016885567.1:p.Gly1712=
NM_004654.4:c.5121A>G MANE Select	NP_004645.2:p.Gly1707=