Canonical Allele Identifier: CA2680116070

Gene: RWDD1

Linked Data

• gnomAD v4: 6-116592901-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116592901A>G , CM000668.2:g.116592901A>G	GRCh38
NC_000006.11:g.116914064A>G , CM000668.1:g.116914064A>G	GRCh37
NC_000006.10:g.117020757A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466444.7:c.611-79A>G MANE Select	ENSP00000420357.2:n.611-79A>G
ENST00000466444.6:c.611-79A>G	ENSP00000420357.2:n.611-79A>G
ENST00000487832.6:c.323-79A>G	ENSP00000428778.1:n.323-79A>G
NM_001007464.2:c.323-79A>G	NP_001007465.1:n.323-79A>G
NM_015952.3:c.611-79A>G	NP_057036.2:n.611-79A>G
NM_016104.3:c.323-79A>G	NP_057188.2:n.323-79A>G
NM_015952.4:c.611-79A>G MANE Select	NP_057036.2:n.611-79A>G
NM_001007464.3:c.323-79A>G	NP_001007465.1:n.323-79A>G
NM_016104.4:c.323-79A>G	NP_057188.2:n.323-79A>G