Canonical Allele Identifier: CA2766241303
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12778361G>C , CM000686.2:g.12778361G>C GRCh38
NC_000024.9:g.14890295G>C , CM000686.1:g.14890295G>C GRCh37
NC_000024.8:g.13399689G>C NCBI36
NG_008311.1:g.82136G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.2880+102G>C ENSP00000498372.1:n.2880+102G>C
ENST00000338981.7:c.2880+102G>C MANE Select ENSP00000342812.3:n.2880+102G>C
ENST00000426564.6:n.2892+102G>C
NM_004654.3:c.2880+102G>C NP_004645.2:n.2880+102G>C
XM_011531469.1:c.2880+102G>C XP_011529771.1:n.2880+102G>C
XM_011531470.1:c.2646+102G>C XP_011529772.1:n.2646+102G>C
XM_017030078.2:c.2895+102G>C XP_016885567.1:n.2895+102G>C
NM_004654.4:c.2880+102G>C MANE Select NP_004645.2:n.2880+102G>C