Canonical Allele Identifier: CA2579747791

Gene: USP9Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12778318_12778319insT , CM000686.2:g.12778318_12778319insT	GRCh38
NC_000024.9:g.14890252_14890253insT , CM000686.1:g.14890252_14890253insT	GRCh37
NC_000024.8:g.13399646_13399647insT	NCBI36
NG_008311.1:g.82093_82094insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.2880+59_2880+60insT	ENSP00000498372.1:n.2880+59_2880+60insT
ENST00000338981.7:c.2880+59_2880+60insT MANE Select	ENSP00000342812.3:n.2880+59_2880+60insT
ENST00000426564.6:n.2892+59_2892+60insT
NM_004654.3:c.2880+59_2880+60insT	NP_004645.2:n.2880+59_2880+60insT
XM_011531469.1:c.2880+59_2880+60insT	XP_011529771.1:n.2880+59_2880+60insT
XM_011531470.1:c.2646+59_2646+60insT	XP_011529772.1:n.2646+59_2646+60insT
XM_017030078.2:c.2895+59_2895+60insT	XP_016885567.1:n.2895+59_2895+60insT
NM_004654.4:c.2880+59_2880+60insT MANE Select	NP_004645.2:n.2880+59_2880+60insT