Canonical Allele Identifier: CA2772740435
Gene: RWDD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116592968_116592969insTTTTTTTTT , CM000668.2:g.116592968_116592969insTTTTTTTTT GRCh38
NC_000006.11:g.116914131_116914132insTTTTTTTTT , CM000668.1:g.116914131_116914132insTTTTTTTTT GRCh37
NC_000006.10:g.117020824_117020825insTTTTTTTTT NCBI36

Transcript Alleles

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