Canonical Allele Identifier: CA2579747940
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810758_12810759insC , CM000686.2:g.12810758_12810759insC GRCh38
NC_000024.9:g.14922693_14922694insC , CM000686.1:g.14922693_14922694insC GRCh37
NC_000024.8:g.13432087_13432088insC NCBI36
NG_008311.1:g.114534_114535insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.4179_4180insC ENSP00000498372.1:p.Asn1394GlnfsTer6
ENST00000338981.7:c.4179_4180insC MANE Select ENSP00000342812.3:p.Asn1394GlnfsTer6
ENST00000426564.6:n.4191_4192insC
NM_004654.3:c.4179_4180insC NP_004645.2:p.Asn1394GlnfsTer6
XM_011531469.1:c.4179_4180insC XP_011529771.1:p.Asn1394GlnfsTer6
XM_011531470.1:c.3945_3946insC XP_011529772.1:p.Asn1316GlnfsTer6
XM_017030078.2:c.4194_4195insC XP_016885567.1:p.Asn1399GlnfsTer6
NM_004654.4:c.4179_4180insC MANE Select NP_004645.2:p.Asn1394GlnfsTer6