Canonical Allele Identifier: CA414984217
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790528A>G , CM000686.2:g.12790528A>G GRCh38
NC_000024.9:g.14902461A>G , CM000686.1:g.14902461A>G GRCh37
NC_000024.8:g.13411855A>G NCBI36
NG_008311.1:g.94302A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.3683A>G ENSP00000498372.1:p.Asn1228Ser
ENST00000338981.7:c.3683A>G MANE Select ENSP00000342812.3:p.Asn1228Ser
ENST00000426564.6:n.3695A>G
NM_004654.3:c.3683A>G NP_004645.2:p.Asn1228Ser
XM_011531469.1:c.3683A>G XP_011529771.1:p.Asn1228Ser
XM_011531470.1:c.3449A>G XP_011529772.1:p.Asn1150Ser
XM_017030078.2:c.3698A>G XP_016885567.1:p.Asn1233Ser
NM_004654.4:c.3683A>G MANE Select NP_004645.2:p.Asn1228Ser