Canonical Allele Identifier: CA365417525

Gene: RWDD1

Linked Data

• MyVariant Identifiers: chr6:g.116914230A>G (hg19) ; chr6:g.116593067A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116593067A>G , CM000668.2:g.116593067A>G	GRCh38
NC_000006.11:g.116914230A>G , CM000668.1:g.116914230A>G	GRCh37
NC_000006.10:g.117020923A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466444.7:c.698A>G MANE Select	ENSP00000420357.2:p.Asn233Ser
ENST00000466444.6:c.698A>G	ENSP00000420357.2:p.Asn233Ser
ENST00000487832.6:c.410A>G	ENSP00000428778.1:p.Asn137Ser
NM_001007464.2:c.410A>G	NP_001007465.1:p.Asn137Ser
NM_015952.3:c.698A>G	NP_057036.2:p.Asn233Ser
NM_016104.3:c.410A>G	NP_057188.2:p.Asn137Ser
NM_015952.4:c.698A>G MANE Select	NP_057036.2:p.Asn233Ser
NM_001007464.3:c.410A>G	NP_001007465.1:p.Asn137Ser
NM_016104.4:c.410A>G	NP_057188.2:p.Asn137Ser