Canonical Allele Identifier: CA337718115

Gene: USP9Y TTTY15

Linked Data

• dbSNP Id: rs990551207
• gnomAD v3: Y-12663131-G-A
• gnomAD v4: Y-12663131-G-A
• MyVariant Identifiers: chrY:g.14775062G>A (hg19) ; chrY:g.12663131G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12663131G>A , CM000686.2:g.12663131G>A	GRCh38
NC_000024.9:g.14775062G>A , CM000686.1:g.14775062G>A	GRCh37
NC_000024.8:g.13284456G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000417071.1:n.170+425G>A
ENST00000440408.5:n.373+425G>A
ENST00000457658.6:n.1004+425G>A (USP9Y)
ENST00000651177.1:c.-248+425G>A (USP9Y)	ENSP00000498372.1:n.-248+425G>A
NR_001545.2:n.340+425G>A (TTTY15)
XR_938612.1:n.490+173C>T
XR_938613.1:n.433+230C>T
XR_002958838.1:n.660+173C>T
XR_002958839.1:n.603+230C>T
NR_001545.3:n.355+425G>A (TTTY15)
NR_174085.1:n.355+425G>A (TTTY15)
NR_174086.1:n.355+425G>A (TTTY15)
NR_174087.1:n.355+425G>A (TTTY15)
NR_174088.1:n.355+425G>A (TTTY15)