Canonical Allele Identifier: CA2558995346
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12777953_12777954insCCA , CM000686.2:g.12777953_12777954insCCA GRCh38
NC_000024.9:g.14889887_14889888insCCA , CM000686.1:g.14889887_14889888insCCA GRCh37
NC_000024.8:g.13399281_13399282insCCA NCBI36
NG_008311.1:g.81728_81729insCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2640-66_2640-65insCCA ENSP00000498372.1:n.2640-66_2640-65insCCA
ENST00000338981.7:c.2640-66_2640-65insCCA MANE Select ENSP00000342812.3:n.2640-66_2640-65insCCA
ENST00000426564.6:n.2652-66_2652-65insCCA
NM_004654.3:c.2640-66_2640-65insCCA NP_004645.2:n.2640-66_2640-65insCCA
XM_011531469.1:c.2640-66_2640-65insCCA XP_011529771.1:n.2640-66_2640-65insCCA
XM_011531470.1:c.2406-66_2406-65insCCA XP_011529772.1:n.2406-66_2406-65insCCA
XM_017030078.2:c.2655-66_2655-65insCCA XP_016885567.1:n.2655-66_2655-65insCCA
NM_004654.4:c.2640-66_2640-65insCCA MANE Select NP_004645.2:n.2640-66_2640-65insCCA