Canonical Allele Identifier: CA2680116099

Gene: RWDD1

Linked Data

• gnomAD v4: 6-116592951-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116592951T>C , CM000668.2:g.116592951T>C	GRCh38
NC_000006.11:g.116914114T>C , CM000668.1:g.116914114T>C	GRCh37
NC_000006.10:g.117020807T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466444.7:c.611-29T>C MANE Select	ENSP00000420357.2:n.611-29T>C
ENST00000466444.6:c.611-29T>C	ENSP00000420357.2:n.611-29T>C
ENST00000487832.6:c.323-29T>C	ENSP00000428778.1:n.323-29T>C
NM_001007464.2:c.323-29T>C	NP_001007465.1:n.323-29T>C
NM_015952.3:c.611-29T>C	NP_057036.2:n.611-29T>C
NM_016104.3:c.323-29T>C	NP_057188.2:n.323-29T>C
NM_015952.4:c.611-29T>C MANE Select	NP_057036.2:n.611-29T>C
NM_001007464.3:c.323-29T>C	NP_001007465.1:n.323-29T>C
NM_016104.4:c.323-29T>C	NP_057188.2:n.323-29T>C