Canonical Allele Identifier: CA1657300383
Gene: RWDD1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116592969G= , CM000668.2:g.116592969G= GRCh38
NC_000006.11:g.116914132G= , CM000668.1:g.116914132G= GRCh37
NC_000006.10:g.117020825G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000466444.7:c.611-11G= MANE Select ENSP00000420357.2:n.611-11G=
ENST00000466444.6:c.611-11G= ENSP00000420357.2:n.611-11G=
ENST00000487832.6:c.323-11G= ENSP00000428778.1:n.323-11G=
NM_001007464.2:c.323-11G= NP_001007465.1:n.323-11G=
NM_015952.3:c.611-11G= NP_057036.2:n.611-11G=
NM_016104.3:c.323-11G= NP_057188.2:n.323-11G=
NM_015952.4:c.611-11G= MANE Select NP_057036.2:n.611-11G=
NM_001007464.3:c.323-11G= NP_001007465.1:n.323-11G=
NM_016104.4:c.323-11G= NP_057188.2:n.323-11G=
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