Canonical Allele Identifier: CA337721236
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs112378995
gnomAD v3: Y-12855767-A-C
gnomAD v4: Y-12855767-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12855767A>C , CM000686.2:g.12855767A>C GRCh38
NC_000024.9:g.14967692A>C , CM000686.1:g.14967692A>C GRCh37
NC_000024.8:g.13477086A>C NCBI36
NG_008311.1:g.159533A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.7065-573A>C ENSP00000498372.1:n.7065-573A>C
ENST00000338981.7:c.7065-573A>C MANE Select ENSP00000342812.3:n.7065-573A>C
ENST00000426564.6:n.7092-573A>C
ENST00000453031.1:c.110-573A>C
NM_004654.3:c.7065-573A>C NP_004645.2:n.7065-573A>C
XM_011531469.1:c.7065-573A>C XP_011529771.1:n.7065-573A>C
XM_011531470.1:c.6831-573A>C XP_011529772.1:n.6831-573A>C
XM_017030078.2:c.7080-573A>C XP_016885567.1:n.7080-573A>C
NM_004654.4:c.7065-573A>C MANE Select NP_004645.2:n.7065-573A>C