Canonical Allele Identifier: CA2739259813

Gene: USP9Y

Linked Data

• dbSNP Id: rs2148291303

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833896T>G , CM000686.2:g.12833896T>G	GRCh38
NC_000024.9:g.14945822T>G , CM000686.1:g.14945822T>G	GRCh37
NC_000024.8:g.13455216T>G	NCBI36
NG_008311.1:g.137663T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.5195+35T>G	ENSP00000498372.1:n.5195+35T>G
ENST00000338981.7:c.5195+35T>G MANE Select	ENSP00000342812.3:n.5195+35T>G
ENST00000426564.6:n.5207+35T>G
NM_004654.3:c.5195+35T>G	NP_004645.2:n.5195+35T>G
XM_011531469.1:c.5195+35T>G	XP_011529771.1:n.5195+35T>G
XM_011531470.1:c.4961+35T>G	XP_011529772.1:n.4961+35T>G
XM_017030078.2:c.5210+35T>G	XP_016885567.1:n.5210+35T>G
NM_004654.4:c.5195+35T>G MANE Select	NP_004645.2:n.5195+35T>G