Canonical Allele Identifier: CA2824885764
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778172_12778173insCACACCCAACAC , CM000686.2:g.12778172_12778173insCACACCCAACAC GRCh38
NC_000024.9:g.14890106_14890107insCACACCCAACAC , CM000686.1:g.14890106_14890107insCACACCCAACAC GRCh37
NC_000024.8:g.13399500_13399501insCACACCCAACAC NCBI36
NG_008311.1:g.81947_81948insCACACCCAACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2793_2794insCACACCCAACAC ENSP00000498372.1:p.Lys931_Lys932insHisThrGlnHis
ENST00000338981.7:c.2793_2794insCACACCCAACAC MANE Select ENSP00000342812.3:p.Lys931_Lys932insHisThrGlnHis
ENST00000426564.6:n.2805_2806insCACACCCAACAC
NM_004654.3:c.2793_2794insCACACCCAACAC NP_004645.2:p.Lys931_Lys932insHisThrGlnHis
XM_011531469.1:c.2793_2794insCACACCCAACAC XP_011529771.1:p.Lys931_Lys932insHisThrGlnHis
XM_011531470.1:c.2559_2560insCACACCCAACAC XP_011529772.1:p.Lys853_Lys854insHisThrGlnHis
XM_017030078.2:c.2808_2809insCACACCCAACAC XP_016885567.1:p.Lys936_Lys937insHisThrGlnHis
NM_004654.4:c.2793_2794insCACACCCAACAC MANE Select NP_004645.2:p.Lys931_Lys932insHisThrGlnHis