Canonical Allele Identifier: CA414989239
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810687A>C , CM000686.2:g.12810687A>C GRCh38
NC_000024.9:g.14922622A>C , CM000686.1:g.14922622A>C GRCh37
NC_000024.8:g.13432016A>C NCBI36
NG_008311.1:g.114463A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4108A>C ENSP00000498372.1:p.Lys1370Gln
ENST00000338981.7:c.4108A>C MANE Select ENSP00000342812.3:p.Lys1370Gln
ENST00000426564.6:n.4120A>C
NM_004654.3:c.4108A>C NP_004645.2:p.Lys1370Gln
XM_011531469.1:c.4108A>C XP_011529771.1:p.Lys1370Gln
XM_011531470.1:c.3874A>C XP_011529772.1:p.Lys1292Gln
XM_017030078.2:c.4123A>C XP_016885567.1:p.Lys1375Gln
NM_004654.4:c.4108A>C MANE Select NP_004645.2:p.Lys1370Gln