Canonical Allele Identifier: CA2541423579
Gene: RWDD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116592928C>T , CM000668.2:g.116592928C>T GRCh38
NC_000006.11:g.116914091C>T , CM000668.1:g.116914091C>T GRCh37
NC_000006.10:g.117020784C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000466444.7:c.611-52C>T MANE Select ENSP00000420357.2:n.611-52C>T
ENST00000466444.6:c.611-52C>T ENSP00000420357.2:n.611-52C>T
ENST00000487832.6:c.323-52C>T ENSP00000428778.1:n.323-52C>T
NM_001007464.2:c.323-52C>T NP_001007465.1:n.323-52C>T
NM_015952.3:c.611-52C>T NP_057036.2:n.611-52C>T
NM_016104.3:c.323-52C>T NP_057188.2:n.323-52C>T
NM_015952.4:c.611-52C>T MANE Select NP_057036.2:n.611-52C>T
NM_001007464.3:c.323-52C>T NP_001007465.1:n.323-52C>T
NM_016104.4:c.323-52C>T NP_057188.2:n.323-52C>T