Canonical Allele Identifier: CA88625834
Gene: USP13 HGNC NCBI

Linked Data

dbSNP Id: rs15241

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179789216C>T , CM000665.2:g.179789216C>T GRCh38
NC_000003.11:g.179507004C>T , CM000665.1:g.179507004C>T GRCh37
NC_000003.10:g.180989698C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000263966.8:c.*5075C>T MANE Select ENSP00000263966.3:n.*5075C>T
ENST00000679407.1:c.155-318C>T ENSP00000506653.1:n.155-318C>T
ENST00000679674.1:c.86-6465C>T
ENST00000679752.1:n.9274C>T
ENST00000679772.1:c.202+4967C>T
ENST00000679972.1:n.6898C>T
ENST00000680008.1:c.2414-13889C>T ENSP00000506330.1:n.2414-13889C>T
ENST00000680549.1:c.86-318C>T
ENST00000680587.1:c.*5075C>T ENSP00000506181.1:n.*5075C>T
ENST00000681262.1:c.155-6465C>T ENSP00000505767.1:n.155-6465C>T
ENST00000681630.1:c.203-318C>T
ENST00000681736.1:c.344+3343C>T
ENST00000681918.1:c.345-318C>T
ENST00000263966.7:c.*5075C>T ENSP00000263966.3:n.*5075C>T
NM_003940.2:c.*5075C>T NP_003931.2:n.*5075C>T
XM_011513269.1:c.*5075C>T XP_011511571.1:n.*5075C>T
NM_003940.3:c.*5075C>T MANE Select NP_003931.2:n.*5075C>T