Canonical Allele Identifier: CA569698011

Gene: RWDD1

Linked Data

• gnomAD v2: 6-116914129-G-GTTTT
• MyVariant Identifiers: chr6:g.116914129_116914130insTTTT (hg19) ; chr6:g.116592966_116592967insTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.116592968_116592969insTTTT , CM000668.2:g.116592968_116592969insTTTT	GRCh38
NC_000006.11:g.116914131_116914132insTTTT , CM000668.1:g.116914131_116914132insTTTT	GRCh37
NC_000006.10:g.117020824_117020825insTTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466444.7:c.611-12_611-11insTTTT MANE Select	ENSP00000420357.2:n.611-12_611-11insTTTT
ENST00000466444.6:c.611-12_611-11insTTTT	ENSP00000420357.2:n.611-12_611-11insTTTT
ENST00000487832.6:c.323-12_323-11insTTTT	ENSP00000428778.1:n.323-12_323-11insTTTT
NM_001007464.2:c.323-12_323-11insTTTT	NP_001007465.1:n.323-12_323-11insTTTT
NM_015952.3:c.611-12_611-11insTTTT	NP_057036.2:n.611-12_611-11insTTTT
NM_016104.3:c.323-12_323-11insTTTT	NP_057188.2:n.323-12_323-11insTTTT
NM_015952.4:c.611-12_611-11insTTTT MANE Select	NP_057036.2:n.611-12_611-11insTTTT
NM_001007464.3:c.323-12_323-11insTTTT	NP_001007465.1:n.323-12_323-11insTTTT
NM_016104.4:c.323-12_323-11insTTTT	NP_057188.2:n.323-12_323-11insTTTT