Canonical Allele Identifier: CA569698010
Gene: RWDD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116592968_116592969insTTT , CM000668.2:g.116592968_116592969insTTT GRCh38
NC_000006.11:g.116914131_116914132insTTT , CM000668.1:g.116914131_116914132insTTT GRCh37
NC_000006.10:g.117020824_117020825insTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000466444.7:c.611-12_611-11insTTT MANE Select ENSP00000420357.2:n.611-12_611-11insTTT
ENST00000466444.6:c.611-12_611-11insTTT ENSP00000420357.2:n.611-12_611-11insTTT
ENST00000487832.6:c.323-12_323-11insTTT ENSP00000428778.1:n.323-12_323-11insTTT
NM_001007464.2:c.323-12_323-11insTTT NP_001007465.1:n.323-12_323-11insTTT
NM_015952.3:c.611-12_611-11insTTT NP_057036.2:n.611-12_611-11insTTT
NM_016104.3:c.323-12_323-11insTTT NP_057188.2:n.323-12_323-11insTTT
NM_015952.4:c.611-12_611-11insTTT MANE Select NP_057036.2:n.611-12_611-11insTTT
NM_001007464.3:c.323-12_323-11insTTT NP_001007465.1:n.323-12_323-11insTTT
NM_016104.4:c.323-12_323-11insTTT NP_057188.2:n.323-12_323-11insTTT