Canonical Allele Identifier: CA385200596

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115497C>A (hg19) ; chr12:g.55721713C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721713C>A , CM000674.2:g.55721713C>A	GRCh38
NC_000012.11:g.56115497C>A , CM000674.1:g.56115497C>A	GRCh37
NC_000012.10:g.54401764C>A	NCBI36
NG_008606.1:g.6347C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.335C>A MANE Select	ENSP00000257895.6:p.Ala112Asp
ENST00000257895.9:c.335C>A	ENSP00000257895.5:p.Ala112Asp
ENST00000257899.3:c.350C>A
ENST00000547072.5:c.44C>A	ENSP00000449927.1:p.Ala15Asp
ENST00000547301.1:n.443C>A
ENST00000548082.1:c.335C>A	ENSP00000447128.1:p.Ala112Asp
ENST00000548123.1:c.300+219C>A
ENST00000548486.1:n.345C>A
ENST00000549424.1:c.*7C>A	ENSP00000447621.1:n.*7C>A
ENST00000550412.5:c.*7C>A	ENSP00000447650.1:n.*7C>A
ENST00000550608.1:n.474C>A
ENST00000551946.5:c.*138C>A	ENSP00000450201.1:n.*138C>A
ENST00000552930.5:c.44C>A	ENSP00000448014.1:p.Ala15Asp
ENST00000553160.1:n.406-482C>A
ENST00000553187.5:n.345C>A
NM_001199771.1:c.335C>A	NP_001186700.1:p.Ala112Asp
NM_002905.3:c.335C>A	NP_002896.2:p.Ala112Asp
NR_037658.1:n.394C>A
NM_001199771.2:c.335C>A	NP_001186700.1:p.Ala112Asp
NM_002905.5:c.335C>A MANE Select	NP_002896.2:p.Ala112Asp
NM_001199771.3:c.335C>A	NP_001186700.1:p.Ala112Asp