Canonical Allele Identifier: CA1139149165
Gene: USP9Y HGNC NCBI
TTTY15 HGNC NCBI

Linked Data

dbSNP Id: rs2053395739
gnomAD v3: Y-12663079-G-A
gnomAD v4: Y-12663079-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12663079G>A , CM000686.2:g.12663079G>A GRCh38
NC_000024.9:g.14775010G>A , CM000686.1:g.14775010G>A GRCh37
NC_000024.8:g.13284404G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000417071.1:n.170+373G>A
ENST00000440408.5:n.373+373G>A
ENST00000457658.6:n.1004+373G>A (USP9Y)
ENST00000651177.1:c.-248+373G>A (USP9Y) ENSP00000498372.1:n.-248+373G>A
NR_001545.2:n.340+373G>A (TTTY15)
XR_938612.1:n.490+225C>T
XR_938613.1:n.433+282C>T
XR_002958838.1:n.660+225C>T
XR_002958839.1:n.603+282C>T
NR_001545.3:n.355+373G>A (TTTY15)
NR_174085.1:n.355+373G>A (TTTY15)
NR_174086.1:n.355+373G>A (TTTY15)
NR_174087.1:n.355+373G>A (TTTY15)
NR_174088.1:n.355+373G>A (TTTY15)