Canonical Allele Identifier: CA1657300377
Gene: RWDD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116592964_116592966delinsTGG , CM000668.2:g.116592964_116592966delinsTGG GRCh38
NC_000006.11:g.116914127_116914129delinsTGG , CM000668.1:g.116914127_116914129delinsTGG GRCh37
NC_000006.10:g.117020820_117020822delinsTGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000466444.7:c.611-16_611-14delinsTGG MANE Select ENSP00000420357.2:n.611-16_611-14delinsTGG
ENST00000466444.6:c.611-16_611-14delinsTGG ENSP00000420357.2:n.611-16_611-14delinsTGG
ENST00000487832.6:c.323-16_323-14delinsTGG ENSP00000428778.1:n.323-16_323-14delinsTGG
NM_001007464.2:c.323-16_323-14delinsTGG NP_001007465.1:n.323-16_323-14delinsTGG
NM_015952.3:c.611-16_611-14delinsTGG NP_057036.2:n.611-16_611-14delinsTGG
NM_016104.3:c.323-16_323-14delinsTGG NP_057188.2:n.323-16_323-14delinsTGG
NM_015952.4:c.611-16_611-14delinsTGG MANE Select NP_057036.2:n.611-16_611-14delinsTGG
NM_001007464.3:c.323-16_323-14delinsTGG NP_001007465.1:n.323-16_323-14delinsTGG
NM_016104.4:c.323-16_323-14delinsTGG NP_057188.2:n.323-16_323-14delinsTGG