Canonical Allele Identifier: CA2772740434
Gene: RWDD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116592968_116592969insTTTTTTTTTTTTTTT , CM000668.2:g.116592968_116592969insTTTTTTTTTTTTTTT GRCh38
NC_000006.11:g.116914131_116914132insTTTTTTTTTTTTTTT , CM000668.1:g.116914131_116914132insTTTTTTTTTTTTTTT GRCh37
NC_000006.10:g.117020824_117020825insTTTTTTTTTTTTTTT NCBI36

Transcript Alleles

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