Canonical Allele Identifier: CA1139149205
Gene: USP9Y HGNC NCBI
TTTY15 HGNC NCBI

Linked Data

gnomAD v3: Y-12663235-A-T
gnomAD v4: Y-12663235-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12663235A>T , CM000686.2:g.12663235A>T GRCh38
NC_000024.9:g.14775166A>T , CM000686.1:g.14775166A>T GRCh37
NC_000024.8:g.13284560A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000417071.1:n.170+529A>T
ENST00000440408.5:n.373+529A>T
ENST00000457658.6:n.1004+529A>T (USP9Y)
ENST00000651177.1:c.-248+529A>T (USP9Y) ENSP00000498372.1:n.-248+529A>T
NR_001545.2:n.340+529A>T (TTTY15)
XR_938612.1:n.490+69T>A
XR_938613.1:n.433+126T>A
XR_002958838.1:n.660+69T>A
XR_002958839.1:n.603+126T>A
NR_001545.3:n.355+529A>T (TTTY15)
NR_174085.1:n.355+529A>T (TTTY15)
NR_174086.1:n.355+529A>T (TTTY15)
NR_174087.1:n.355+529A>T (TTTY15)
NR_174088.1:n.355+529A>T (TTTY15)