Canonical Allele Identifier: CA337718116
Gene: USP9Y HGNC NCBI
TTTY15 HGNC NCBI

Linked Data

dbSNP Id: rs764133217
gnomAD v3: Y-12663133-G-T
gnomAD v4: Y-12663133-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12663133G>T , CM000686.2:g.12663133G>T GRCh38
NC_000024.9:g.14775064G>T , CM000686.1:g.14775064G>T GRCh37
NC_000024.8:g.13284458G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000417071.1:n.170+427G>T
ENST00000440408.5:n.373+427G>T
ENST00000457658.6:n.1004+427G>T (USP9Y)
ENST00000651177.1:c.-248+427G>T (USP9Y) ENSP00000498372.1:n.-248+427G>T
NR_001545.2:n.340+427G>T (TTTY15)
XR_938612.1:n.490+171C>A
XR_938613.1:n.433+228C>A
XR_002958838.1:n.660+171C>A
XR_002958839.1:n.603+228C>A
NR_001545.3:n.355+427G>T (TTTY15)
NR_174085.1:n.355+427G>T (TTTY15)
NR_174086.1:n.355+427G>T (TTTY15)
NR_174087.1:n.355+427G>T (TTTY15)
NR_174088.1:n.355+427G>T (TTTY15)