Canonical Allele Identifier: CA385200990

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115643A>T (hg19) ; chr12:g.55721859A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721859A>T , CM000674.2:g.55721859A>T	GRCh38
NC_000012.11:g.56115643A>T , CM000674.1:g.56115643A>T	GRCh37
NC_000012.10:g.54401910A>T	NCBI36
NG_008606.1:g.6493A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.481A>T MANE Select	ENSP00000257895.6:p.Ile161Phe
ENST00000257895.9:c.481A>T	ENSP00000257895.5:p.Ile161Phe
ENST00000257899.3:c.496A>T
ENST00000547072.5:c.190A>T	ENSP00000449927.1:p.Ile64Phe
ENST00000548082.1:c.481A>T	ENSP00000447128.1:p.Ile161Phe
ENST00000548123.1:c.300+365A>T
ENST00000548486.1:n.491A>T
ENST00000550412.5:c.*153A>T	ENSP00000447650.1:n.*153A>T
ENST00000550608.1:n.620A>T
ENST00000551946.5:c.*284A>T	ENSP00000450201.1:n.*284A>T
ENST00000553160.1:n.406-336A>T
ENST00000553187.5:n.491A>T
NM_001199771.1:c.481A>T	NP_001186700.1:p.Ile161Phe
NM_002905.3:c.481A>T	NP_002896.2:p.Ile161Phe
NR_037658.1:n.540A>T
NM_001199771.2:c.481A>T	NP_001186700.1:p.Ile161Phe
NM_002905.5:c.481A>T MANE Select	NP_002896.2:p.Ile161Phe
NM_001199771.3:c.481A>T	NP_001186700.1:p.Ile161Phe