Canonical Allele Identifier: CA2824887622
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12857695_12857696insAAACCAAACACACCCAACA , CM000686.2:g.12857695_12857696insAAACCAAACACACCCAACA GRCh38
NC_000024.9:g.14969620_14969621insAAACCAAACACACCCAACA , CM000686.1:g.14969620_14969621insAAACCAAACACACCCAACA GRCh37
NC_000024.8:g.13479014_13479015insAAACCAAACACACCCAACA NCBI36
NG_008311.1:g.161461_161462insAAACCAAACACACCCAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.7530+34_7530+35insAAACCAAACACACCCAACA ENSP00000498372.1:n.7530+34_7530+35insAAACCAAACACACCCAACA
ENST00000338981.7:c.7530+34_7530+35insAAACCAAACACACCCAACA MANE Select ENSP00000342812.3:n.7530+34_7530+35insAAACCAAACACACCCAACA
ENST00000426564.6:n.7557+34_7557+35insAAACCAAACACACCCAACA
ENST00000453031.1:c.575+34_575+35insAAACCAAACACACCCAACA
ENST00000471409.1:n.849+34_849+35insAAACCAAACACACCCAACA
NM_004654.3:c.7530+34_7530+35insAAACCAAACACACCCAACA NP_004645.2:n.7530+34_7530+35insAAACCAAACACACCCAACA
XM_011531469.1:c.7530+34_7530+35insAAACCAAACACACCCAACA XP_011529771.1:n.7530+34_7530+35insAAACCAAACACACCCAACA
XM_011531470.1:c.7296+34_7296+35insAAACCAAACACACCCAACA XP_011529772.1:n.7296+34_7296+35insAAACCAAACACACCCAACA
XM_017030078.2:c.7545+34_7545+35insAAACCAAACACACCCAACA XP_016885567.1:n.7545+34_7545+35insAAACCAAACACACCCAACA
NM_004654.4:c.7530+34_7530+35insAAACCAAACACACCCAACA MANE Select NP_004645.2:n.7530+34_7530+35insAAACCAAACACACCCAACA