Canonical Allele Identifier: CA365417580

Gene: RWDD1

Linked Data

• MyVariant Identifiers: chr6:g.116914239A>T (hg19) ; chr6:g.116593076A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116593076A>T , CM000668.2:g.116593076A>T	GRCh38
NC_000006.11:g.116914239A>T , CM000668.1:g.116914239A>T	GRCh37
NC_000006.10:g.117020932A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466444.7:c.707A>T MANE Select	ENSP00000420357.2:p.Asp236Val
ENST00000466444.6:c.707A>T	ENSP00000420357.2:p.Asp236Val
ENST00000487832.6:c.419A>T	ENSP00000428778.1:p.Asp140Val
NM_001007464.2:c.419A>T	NP_001007465.1:p.Asp140Val
NM_015952.3:c.707A>T	NP_057036.2:p.Asp236Val
NM_016104.3:c.419A>T	NP_057188.2:p.Asp140Val
NM_015952.4:c.707A>T MANE Select	NP_057036.2:p.Asp236Val
NM_001007464.3:c.419A>T	NP_001007465.1:p.Asp140Val
NM_016104.4:c.419A>T	NP_057188.2:p.Asp140Val