Canonical Allele Identifier: CA385200564

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115489G>C (hg19) ; chr12:g.55721705G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721705G>C , CM000674.2:g.55721705G>C	GRCh38
NC_000012.11:g.56115489G>C , CM000674.1:g.56115489G>C	GRCh37
NC_000012.10:g.54401756G>C	NCBI36
NG_008606.1:g.6339G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.327G>C MANE Select	ENSP00000257895.6:p.Val109=
ENST00000257895.9:c.327G>C	ENSP00000257895.5:p.Val109=
ENST00000257899.3:c.342G>C
ENST00000547072.5:c.36G>C	ENSP00000449927.1:p.Val12=
ENST00000547301.1:n.435G>C
ENST00000548082.1:c.327G>C	ENSP00000447128.1:p.Val109=
ENST00000548123.1:c.300+211G>C
ENST00000548486.1:n.337G>C
ENST00000549424.1:c.134G>C	ENSP00000447621.1:p.Ter45Ser
ENST00000550412.5:c.368G>C	ENSP00000447650.1:p.Ter123Ser
ENST00000550608.1:n.466G>C
ENST00000551946.5:c.*130G>C	ENSP00000450201.1:n.*130G>C
ENST00000552930.5:c.36G>C	ENSP00000448014.1:p.Val12=
ENST00000553160.1:n.406-490G>C
ENST00000553187.5:n.337G>C
NM_001199771.1:c.327G>C	NP_001186700.1:p.Val109=
NM_002905.3:c.327G>C	NP_002896.2:p.Val109=
NR_037658.1:n.386G>C
NM_001199771.2:c.327G>C	NP_001186700.1:p.Val109=
NM_002905.5:c.327G>C MANE Select	NP_002896.2:p.Val109=
NM_001199771.3:c.327G>C	NP_001186700.1:p.Val109=