Canonical Allele Identifier: CA10573495

Gene: USP9Y

Linked Data

• dbSNP Id: rs778269364
• ExAC: Y:14958226 T / C
• gnomAD v2: Y-14958226-T-C
• MyVariant Identifiers: chrY:g.14958226T>C (hg19) ; chrY:g.12846301T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12846301T>C , CM000686.2:g.12846301T>C	GRCh38
NC_000024.9:g.14958226T>C , CM000686.1:g.14958226T>C	GRCh37
NC_000024.8:g.13467620T>C	NCBI36
NG_008311.1:g.150067T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.6569-32T>C	ENSP00000498372.1:n.6569-32T>C
ENST00000338981.7:c.6569-32T>C MANE Select	ENSP00000342812.3:n.6569-32T>C
ENST00000426564.6:n.6596-32T>C
NM_004654.3:c.6569-32T>C	NP_004645.2:n.6569-32T>C
XM_011531469.1:c.6569-32T>C	XP_011529771.1:n.6569-32T>C
XM_011531470.1:c.6335-32T>C	XP_011529772.1:n.6335-32T>C
XM_017030078.2:c.6584-32T>C	XP_016885567.1:n.6584-32T>C
NM_004654.4:c.6569-32T>C MANE Select	NP_004645.2:n.6569-32T>C