Canonical Allele Identifier: CA2470560464

Gene: USP9Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833900_12833901delinsGT , CM000686.2:g.12833900_12833901delinsGT	GRCh38
NC_000024.9:g.14945826_14945827delinsGT , CM000686.1:g.14945826_14945827delinsGT	GRCh37
NC_000024.8:g.13455220_13455221delinsGT	NCBI36
NG_008311.1:g.137667_137668delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.5195+39_5195+40delinsGT	ENSP00000498372.1:n.5195+39_5195+40delinsGT
ENST00000338981.7:c.5195+39_5195+40delinsGT MANE Select	ENSP00000342812.3:n.5195+39_5195+40delinsGT
ENST00000426564.6:n.5207+39_5207+40delinsGT
NM_004654.3:c.5195+39_5195+40delinsGT	NP_004645.2:n.5195+39_5195+40delinsGT
XM_011531469.1:c.5195+39_5195+40delinsGT	XP_011529771.1:n.5195+39_5195+40delinsGT
XM_011531470.1:c.4961+39_4961+40delinsGT	XP_011529772.1:n.4961+39_4961+40delinsGT
XM_017030078.2:c.5210+39_5210+40delinsGT	XP_016885567.1:n.5210+39_5210+40delinsGT
NM_004654.4:c.5195+39_5195+40delinsGT MANE Select	NP_004645.2:n.5195+39_5195+40delinsGT