Canonical Allele Identifier: CA2470555351
Gene: USP9Y HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735789_12735794delinsATTAAG , CM000686.2:g.12735789_12735794delinsATTAAG GRCh38
NC_000024.9:g.14847723_14847728delinsATTAAG , CM000686.1:g.14847723_14847728delinsATTAAG GRCh37
NC_000024.8:g.13357117_13357122delinsATTAAG NCBI36
NG_008311.1:g.39564_39569delinsATTAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.773+62_773+67delinsATTAAG ENSP00000498372.1:n.773+62_773+67delinsAT...
ENST00000338981.7:c.773+62_773+67delinsATTAAG MANE Select ENSP00000342812.3:n.773+62_773+67delinsAT...
ENST00000426564.6:n.785+62_785+67delinsATTAAG
NM_004654.3:c.773+62_773+67delinsATTAAG NP_004645.2:n.773+62_773+67delinsATTAAG
XM_011531469.1:c.773+62_773+67delinsATTAAG XP_011529771.1:n.773+62_773+67delinsATTAA...
XM_011531470.1:c.535_539+1delinsATTAAG
XM_017030078.2:c.773+62_773+67delinsATTAAG XP_016885567.1:n.773+62_773+67delinsATTAA...
NM_004654.4:c.773+62_773+67delinsATTAAG MANE Select NP_004645.2:n.773+62_773+67delinsATTAAG