Canonical Allele Identifier: CA414983967
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12790493A>C , CM000686.2:g.12790493A>C GRCh38
NC_000024.9:g.14902426A>C , CM000686.1:g.14902426A>C GRCh37
NC_000024.8:g.13411820A>C NCBI36
NG_008311.1:g.94267A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.3648A>C ENSP00000498372.1:p.Arg1216Ser
ENST00000338981.7:c.3648A>C MANE Select ENSP00000342812.3:p.Arg1216Ser
ENST00000426564.6:n.3660A>C
NM_004654.3:c.3648A>C NP_004645.2:p.Arg1216Ser
XM_011531469.1:c.3648A>C XP_011529771.1:p.Arg1216Ser
XM_011531470.1:c.3414A>C XP_011529772.1:p.Arg1138Ser
XM_017030078.2:c.3663A>C XP_016885567.1:p.Arg1221Ser
NM_004654.4:c.3648A>C MANE Select NP_004645.2:p.Arg1216Ser