Canonical Allele Identifier: CA1657300324

Gene: RWDD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116592864C= , CM000668.2:g.116592864C=	GRCh38
NC_000006.11:g.116914027C= , CM000668.1:g.116914027C=	GRCh37
NC_000006.10:g.117020720C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466444.7:c.611-116C= MANE Select	ENSP00000420357.2:n.611-116C=
ENST00000466444.6:c.611-116C=	ENSP00000420357.2:n.611-116C=
ENST00000487832.6:c.323-116C=	ENSP00000428778.1:n.323-116C=
NM_001007464.2:c.323-116C=	NP_001007465.1:n.323-116C=
NM_015952.3:c.611-116C=	NP_057036.2:n.611-116C=
NM_016104.3:c.323-116C=	NP_057188.2:n.323-116C=
NM_015952.4:c.611-116C= MANE Select	NP_057036.2:n.611-116C=
NM_001007464.3:c.323-116C=	NP_001007465.1:n.323-116C=
NM_016104.4:c.323-116C=	NP_057188.2:n.323-116C=