Canonical Allele Identifier: CA1657300378
Gene: RWDD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116592964_116592971delinsTGGTTGCC , CM000668.2:g.116592964_116592971delinsTGGTTGCC GRCh38
NC_000006.11:g.116914127_116914134delinsTGGTTGCC , CM000668.1:g.116914127_116914134delinsTGGTTGCC GRCh37
NC_000006.10:g.117020820_117020827delinsTGGTTGCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000466444.7:c.611-16_611-9delinsTGGTTGCC MANE Select ENSP00000420357.2:n.611-16_611-9delinsTGGTTGCC
ENST00000466444.6:c.611-16_611-9delinsTGGTTGCC ENSP00000420357.2:n.611-16_611-9delinsTGGTTGCC
ENST00000487832.6:c.323-16_323-9delinsTGGTTGCC ENSP00000428778.1:n.323-16_323-9delinsTGGTTGCC
NM_001007464.2:c.323-16_323-9delinsTGGTTGCC NP_001007465.1:n.323-16_323-9delinsTGGTTGCC
NM_015952.3:c.611-16_611-9delinsTGGTTGCC NP_057036.2:n.611-16_611-9delinsTGGTTGCC
NM_016104.3:c.323-16_323-9delinsTGGTTGCC NP_057188.2:n.323-16_323-9delinsTGGTTGCC
NM_015952.4:c.611-16_611-9delinsTGGTTGCC MANE Select NP_057036.2:n.611-16_611-9delinsTGGTTGCC
NM_001007464.3:c.323-16_323-9delinsTGGTTGCC NP_001007465.1:n.323-16_323-9delinsTGGTTGCC
NM_016104.4:c.323-16_323-9delinsTGGTTGCC NP_057188.2:n.323-16_323-9delinsTGGTTGCC