Canonical Allele Identifier: CA480155969

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115675T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721891T>C , CM000674.2:g.55721891T>C	GRCh38
NC_000012.11:g.56115675T>C , CM000674.1:g.56115675T>C	GRCh37
NC_000012.10:g.54401942T>C	NCBI36
NG_008606.1:g.6525T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.513T>C MANE Select	ENSP00000257895.6:p.Asn171=
ENST00000257895.9:c.513T>C	ENSP00000257895.5:p.Asn171=
ENST00000257899.3:c.528T>C
ENST00000547072.5:c.222T>C	ENSP00000449927.1:p.Asn74=
ENST00000548082.1:c.513T>C	ENSP00000447128.1:p.Asn171=
ENST00000548123.1:c.300+397T>C
ENST00000548486.1:n.523T>C
ENST00000550412.5:c.*185T>C	ENSP00000447650.1:n.*185T>C
ENST00000550608.1:n.652T>C
ENST00000551946.5:c.*316T>C	ENSP00000450201.1:n.*316T>C
ENST00000553160.1:n.406-304T>C
ENST00000553187.5:n.523T>C
NM_001199771.1:c.513T>C	NP_001186700.1:p.Asn171=
NM_002905.3:c.513T>C	NP_002896.2:p.Asn171=
NR_037658.1:n.572T>C
NM_001199771.2:c.513T>C	NP_001186700.1:p.Asn171=
NM_002905.5:c.513T>C MANE Select	NP_002896.2:p.Asn171=
NM_001199771.3:c.513T>C	NP_001186700.1:p.Asn171=