Canonical Allele Identifier: CA414989806
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs1374020988
gnomAD v2: Y-14922682-A-G
gnomAD v3: Y-12810747-A-G
gnomAD v4: Y-12810747-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810747A>G , CM000686.2:g.12810747A>G GRCh38
NC_000024.9:g.14922682A>G , CM000686.1:g.14922682A>G GRCh37
NC_000024.8:g.13432076A>G NCBI36
NG_008311.1:g.114523A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.4168A>G ENSP00000498372.1:p.Asn1390Asp
ENST00000338981.7:c.4168A>G MANE Select ENSP00000342812.3:p.Asn1390Asp
ENST00000426564.6:n.4180A>G
NM_004654.3:c.4168A>G NP_004645.2:p.Asn1390Asp
XM_011531469.1:c.4168A>G XP_011529771.1:p.Asn1390Asp
XM_011531470.1:c.3934A>G XP_011529772.1:p.Asn1312Asp
XM_017030078.2:c.4183A>G XP_016885567.1:p.Asn1395Asp
NM_004654.4:c.4168A>G MANE Select NP_004645.2:p.Asn1390Asp