Canonical Allele Identifier: CA10573189

Gene: USP9Y

Linked Data

• dbSNP Id: rs760941053
• ExAC: Y:14889920 A / T
• gnomAD v2: Y-14889920-A-T
• MyVariant Identifiers: chrY:g.14889920A>T (hg19) ; chrY:g.12777986A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12777986A>T , CM000686.2:g.12777986A>T	GRCh38
NC_000024.9:g.14889920A>T , CM000686.1:g.14889920A>T	GRCh37
NC_000024.8:g.13399314A>T	NCBI36
NG_008311.1:g.81761A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.2640-33A>T	ENSP00000498372.1:n.2640-33A>T
ENST00000338981.7:c.2640-33A>T MANE Select	ENSP00000342812.3:n.2640-33A>T
ENST00000426564.6:n.2652-33A>T
NM_004654.3:c.2640-33A>T	NP_004645.2:n.2640-33A>T
XM_011531469.1:c.2640-33A>T	XP_011529771.1:n.2640-33A>T
XM_011531470.1:c.2406-33A>T	XP_011529772.1:n.2406-33A>T
XM_017030078.2:c.2655-33A>T	XP_016885567.1:n.2655-33A>T
NM_004654.4:c.2640-33A>T MANE Select	NP_004645.2:n.2640-33A>T