Canonical Allele Identifier: CA2470560463

Gene: USP9Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12833899_12833900delinsTG , CM000686.2:g.12833899_12833900delinsTG	GRCh38
NC_000024.9:g.14945825_14945826delinsTG , CM000686.1:g.14945825_14945826delinsTG	GRCh37
NC_000024.8:g.13455219_13455220delinsTG	NCBI36
NG_008311.1:g.137666_137667delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651177.1:c.5195+38_5195+39delinsTG	ENSP00000498372.1:n.5195+38_5195+39delinsTG
ENST00000338981.7:c.5195+38_5195+39delinsTG MANE Select	ENSP00000342812.3:n.5195+38_5195+39delinsTG
ENST00000426564.6:n.5207+38_5207+39delinsTG
NM_004654.3:c.5195+38_5195+39delinsTG	NP_004645.2:n.5195+38_5195+39delinsTG
XM_011531469.1:c.5195+38_5195+39delinsTG	XP_011529771.1:n.5195+38_5195+39delinsTG
XM_011531470.1:c.4961+38_4961+39delinsTG	XP_011529772.1:n.4961+38_4961+39delinsTG
XM_017030078.2:c.5210+38_5210+39delinsTG	XP_016885567.1:n.5210+38_5210+39delinsTG
NM_004654.4:c.5195+38_5195+39delinsTG MANE Select	NP_004645.2:n.5195+38_5195+39delinsTG