Canonical Allele Identifier: CA1139183188
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs2053494157
gnomAD v3: Y-12777971-G-T
gnomAD v4: Y-12777971-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12777971G>T , CM000686.2:g.12777971G>T GRCh38
NC_000024.9:g.14889905G>T , CM000686.1:g.14889905G>T GRCh37
NC_000024.8:g.13399299G>T NCBI36
NG_008311.1:g.81746G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2640-48G>T ENSP00000498372.1:n.2640-48G>T
ENST00000338981.7:c.2640-48G>T MANE Select ENSP00000342812.3:n.2640-48G>T
ENST00000426564.6:n.2652-48G>T
NM_004654.3:c.2640-48G>T NP_004645.2:n.2640-48G>T
XM_011531469.1:c.2640-48G>T XP_011529771.1:n.2640-48G>T
XM_011531470.1:c.2406-48G>T XP_011529772.1:n.2406-48G>T
XM_017030078.2:c.2655-48G>T XP_016885567.1:n.2655-48G>T
NM_004654.4:c.2640-48G>T MANE Select NP_004645.2:n.2640-48G>T