Canonical Allele Identifier: CA880344975

Gene: USP9Y

Linked Data

• dbSNP Id: rs1303252947
• MyVariant Identifiers: chrY:g.14930137del (hg19) ; chrY:g.12818202del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12818208del , CM000686.2:g.12818208del	GRCh38
NC_000024.9:g.14930143del , CM000686.1:g.14930143del	GRCh37
NC_000024.8:g.13439537del	NCBI36
NG_008311.1:g.121984del

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.4831-212del	ENSP00000498372.1:n.4831-212del
ENST00000338981.7:c.4831-212del MANE Select	ENSP00000342812.3:n.4831-212del
ENST00000426564.6:n.4843-212del
NM_004654.3:c.4831-212del	NP_004645.2:n.4831-212del
XM_011531469.1:c.4831-212del	XP_011529771.1:n.4831-212del
XM_011531470.1:c.4597-212del	XP_011529772.1:n.4597-212del
XM_017030078.2:c.4846-212del	XP_016885567.1:n.4846-212del
NM_004654.4:c.4831-212del MANE Select	NP_004645.2:n.4831-212del