Canonical Allele Identifier: CA385200616

Gene: RDH5

Linked Data

• gnomAD v4: 12-55721721-G-T
• MyVariant Identifiers: chr12:g.56115505G>T (hg19) ; chr12:g.55721721G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721721G>T , CM000674.2:g.55721721G>T	GRCh38
NC_000012.11:g.56115505G>T , CM000674.1:g.56115505G>T	GRCh37
NC_000012.10:g.54401772G>T	NCBI36
NG_008606.1:g.6355G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.343G>T MANE Select	ENSP00000257895.6:p.Ala115Ser
ENST00000257895.9:c.343G>T	ENSP00000257895.5:p.Ala115Ser
ENST00000257899.3:c.358G>T
ENST00000547072.5:c.52G>T	ENSP00000449927.1:p.Ala18Ser
ENST00000547301.1:n.451G>T
ENST00000548082.1:c.343G>T	ENSP00000447128.1:p.Ala115Ser
ENST00000548123.1:c.300+227G>T
ENST00000548486.1:n.353G>T
ENST00000549424.1:c.*15G>T	ENSP00000447621.1:n.*15G>T
ENST00000550412.5:c.*15G>T	ENSP00000447650.1:n.*15G>T
ENST00000550608.1:n.482G>T
ENST00000551946.5:c.*146G>T	ENSP00000450201.1:n.*146G>T
ENST00000552930.5:c.52G>T	ENSP00000448014.1:p.Ala18Ser
ENST00000553160.1:n.406-474G>T
ENST00000553187.5:n.353G>T
NM_001199771.1:c.343G>T	NP_001186700.1:p.Ala115Ser
NM_002905.3:c.343G>T	NP_002896.2:p.Ala115Ser
NR_037658.1:n.402G>T
NM_001199771.2:c.343G>T	NP_001186700.1:p.Ala115Ser
NM_002905.5:c.343G>T MANE Select	NP_002896.2:p.Ala115Ser
NM_001199771.3:c.343G>T	NP_001186700.1:p.Ala115Ser