Canonical Allele Identifier: CA337721265

Gene: USP9Y

Linked Data

• dbSNP Id: rs751463196
• gnomAD v3: Y-12857765-T-C
• gnomAD v4: Y-12857765-T-C
• MyVariant Identifiers: chrY:g.14969690T>C (hg19) ; chrY:g.12857765T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12857765T>C , CM000686.2:g.12857765T>C	GRCh38
NC_000024.9:g.14969690T>C , CM000686.1:g.14969690T>C	GRCh37
NC_000024.8:g.13479084T>C	NCBI36
NG_008311.1:g.161531T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.7530+104T>C	ENSP00000498372.1:n.7530+104T>C
ENST00000338981.7:c.7530+104T>C MANE Select	ENSP00000342812.3:n.7530+104T>C
ENST00000426564.6:n.7557+104T>C
ENST00000453031.1:c.575+104T>C
ENST00000471409.1:n.849+104T>C
NM_004654.3:c.7530+104T>C	NP_004645.2:n.7530+104T>C
XM_011531469.1:c.7530+104T>C	XP_011529771.1:n.7530+104T>C
XM_011531470.1:c.7296+104T>C	XP_011529772.1:n.7296+104T>C
XM_017030078.2:c.7545+104T>C	XP_016885567.1:n.7545+104T>C
NM_004654.4:c.7530+104T>C MANE Select	NP_004645.2:n.7530+104T>C