Canonical Allele Identifier: CA415008266

Gene: USP9Y

Linked Data

• MyVariant Identifiers: chrY:g.14890057C>G (hg19) ; chrY:g.12778123C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778123C>G , CM000686.2:g.12778123C>G	GRCh38
NC_000024.9:g.14890057C>G , CM000686.1:g.14890057C>G	GRCh37
NC_000024.8:g.13399451C>G	NCBI36
NG_008311.1:g.81898C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2744C>G	ENSP00000498372.1:p.Ser915Ter
ENST00000338981.7:c.2744C>G MANE Select	ENSP00000342812.3:p.Ser915Ter
ENST00000426564.6:n.2756C>G
NM_004654.3:c.2744C>G	NP_004645.2:p.Ser915Ter
XM_011531469.1:c.2744C>G	XP_011529771.1:p.Ser915Ter
XM_011531470.1:c.2510C>G	XP_011529772.1:p.Ser837Ter
XM_017030078.2:c.2759C>G	XP_016885567.1:p.Ser920Ter
NM_004654.4:c.2744C>G MANE Select	NP_004645.2:p.Ser915Ter