Canonical Allele Identifier: CA414989259
Gene: USP9Y HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810689G>C , CM000686.2:g.12810689G>C GRCh38
NC_000024.9:g.14922624G>C , CM000686.1:g.14922624G>C GRCh37
NC_000024.8:g.13432018G>C NCBI36
NG_008311.1:g.114465G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4110G>C ENSP00000498372.1:p.Lys1370Asn
ENST00000338981.7:c.4110G>C MANE Select ENSP00000342812.3:p.Lys1370Asn
ENST00000426564.6:n.4122G>C
NM_004654.3:c.4110G>C NP_004645.2:p.Lys1370Asn
XM_011531469.1:c.4110G>C XP_011529771.1:p.Lys1370Asn
XM_011531470.1:c.3876G>C XP_011529772.1:p.Lys1292Asn
XM_017030078.2:c.4125G>C XP_016885567.1:p.Lys1375Asn
NM_004654.4:c.4110G>C MANE Select NP_004645.2:p.Lys1370Asn