Canonical Allele Identifier: CA645286648

Gene: USP9Y

Linked Data

• dbSNP Id: rs1415383865
• gnomAD v2: Y-14958249-T-G
• MyVariant Identifiers: chrY:g.14958249T>G (hg19) ; chrY:g.12846324T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12846324T>G , CM000686.2:g.12846324T>G	GRCh38
NC_000024.9:g.14958249T>G , CM000686.1:g.14958249T>G	GRCh37
NC_000024.8:g.13467643T>G	NCBI36
NG_008311.1:g.150090T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.6569-9T>G	ENSP00000498372.1:n.6569-9T>G
ENST00000338981.7:c.6569-9T>G MANE Select	ENSP00000342812.3:n.6569-9T>G
ENST00000426564.6:n.6596-9T>G
NM_004654.3:c.6569-9T>G	NP_004645.2:n.6569-9T>G
XM_011531469.1:c.6569-9T>G	XP_011529771.1:n.6569-9T>G
XM_011531470.1:c.6335-9T>G	XP_011529772.1:n.6335-9T>G
XM_017030078.2:c.6584-9T>G	XP_016885567.1:n.6584-9T>G
NM_004654.4:c.6569-9T>G MANE Select	NP_004645.2:n.6569-9T>G