Canonical Allele Identifier: CA2578721770
Gene: RWDD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116592924del , CM000668.2:g.116592924del GRCh38
NC_000006.11:g.116914087del , CM000668.1:g.116914087del GRCh37
NC_000006.10:g.117020780del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000466444.7:c.611-56del MANE Select ENSP00000420357.2:n.611-56del
ENST00000466444.6:c.611-56del ENSP00000420357.2:n.611-56del
ENST00000487832.6:c.323-56del ENSP00000428778.1:n.323-56del
NM_001007464.2:c.323-56del NP_001007465.1:n.323-56del
NM_015952.3:c.611-56del NP_057036.2:n.611-56del
NM_016104.3:c.323-56del NP_057188.2:n.323-56del
NM_015952.4:c.611-56del MANE Select NP_057036.2:n.611-56del
NM_001007464.3:c.323-56del NP_001007465.1:n.323-56del
NM_016104.4:c.323-56del NP_057188.2:n.323-56del