Canonical Allele Identifier: CA2680116054
Gene: RWDD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116592874_116592875del , CM000668.2:g.116592874_116592875del GRCh38
NC_000006.11:g.116914037_116914038del , CM000668.1:g.116914037_116914038del GRCh37
NC_000006.10:g.117020730_117020731del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000466444.7:c.611-106_611-105del MANE Select ENSP00000420357.2:n.611-106_611-105del
ENST00000466444.6:c.611-106_611-105del ENSP00000420357.2:n.611-106_611-105del
ENST00000487832.6:c.323-106_323-105del ENSP00000428778.1:n.323-106_323-105del
NM_001007464.2:c.323-106_323-105del NP_001007465.1:n.323-106_323-105del
NM_015952.3:c.611-106_611-105del NP_057036.2:n.611-106_611-105del
NM_016104.3:c.323-106_323-105del NP_057188.2:n.323-106_323-105del
NM_015952.4:c.611-106_611-105del MANE Select NP_057036.2:n.611-106_611-105del
NM_001007464.3:c.323-106_323-105del NP_001007465.1:n.323-106_323-105del
NM_016104.4:c.323-106_323-105del NP_057188.2:n.323-106_323-105del