Canonical Allele Identifier: CA1139263938
Gene: USP9Y HGNC NCBI

Linked Data

gnomAD v3: Y-12810646-C-G
gnomAD v4: Y-12810646-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810646C>G , CM000686.2:g.12810646C>G GRCh38
NC_000024.9:g.14922581C>G , CM000686.1:g.14922581C>G GRCh37
NC_000024.8:g.13431975C>G NCBI36
NG_008311.1:g.114422C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4093-26C>G ENSP00000498372.1:n.4093-26C>G
ENST00000338981.7:c.4093-26C>G MANE Select ENSP00000342812.3:n.4093-26C>G
ENST00000426564.6:n.4105-26C>G
NM_004654.3:c.4093-26C>G NP_004645.2:n.4093-26C>G
XM_011531469.1:c.4093-26C>G XP_011529771.1:n.4093-26C>G
XM_011531470.1:c.3859-26C>G XP_011529772.1:n.3859-26C>G
XM_017030078.2:c.4108-26C>G XP_016885567.1:n.4108-26C>G
NM_004654.4:c.4093-26C>G MANE Select NP_004645.2:n.4093-26C>G