Canonical Allele Identifier: CA1139769261

Gene: USP9Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12735899_12735900delinsTT , CM000686.2:g.12735899_12735900delinsTT	GRCh38
NC_000024.9:g.14847833_14847834delinsTT , CM000686.1:g.14847833_14847834delinsTT	GRCh37
NC_000024.8:g.13357227_13357228delinsTT	NCBI36
NG_008311.1:g.39674_39675delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000651177.1:c.774-99_774-98delinsTT	ENSP00000498372.1:n.774-99_774-98delinsTT...
ENST00000338981.7:c.774-99_774-98delinsTT MANE Select	ENSP00000342812.3:n.774-99_774-98delinsTT...
ENST00000426564.6:n.786-99_786-98delinsTT
NM_004654.3:c.774-99_774-98delinsTT	NP_004645.2:n.774-99_774-98delinsTT
XM_011531469.1:c.774-99_774-98delinsTT	XP_011529771.1:n.774-99_774-98delinsTT
XM_011531470.1:c.540-99_540-98delinsTT	XP_011529772.1:n.540-99_540-98delinsTT
XM_017030078.2:c.774-99_774-98delinsTT	XP_016885567.1:n.774-99_774-98delinsTT
NM_004654.4:c.774-99_774-98delinsTT MANE Select	NP_004645.2:n.774-99_774-98delinsTT