Canonical Allele Identifier: CA480156259

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115723C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721939C>T , CM000674.2:g.55721939C>T	GRCh38
NC_000012.11:g.56115723C>T , CM000674.1:g.56115723C>T	GRCh37
NC_000012.10:g.54401990C>T	NCBI36
NG_008606.1:g.6573C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.561C>T MANE Select	ENSP00000257895.6:p.Asp187=
ENST00000257895.9:c.561C>T	ENSP00000257895.5:p.Asp187=
ENST00000257899.3:c.576C>T
ENST00000547072.5:c.270C>T	ENSP00000449927.1:p.Asp90=
ENST00000548082.1:c.561C>T	ENSP00000447128.1:p.Asp187=
ENST00000548123.1:c.300+445C>T
ENST00000548486.1:n.571C>T
ENST00000550412.5:c.*233C>T	ENSP00000447650.1:n.*233C>T
ENST00000550608.1:n.700C>T
ENST00000551946.5:c.*364C>T	ENSP00000450201.1:n.*364C>T
ENST00000553160.1:n.406-256C>T
ENST00000553187.5:n.571C>T
NM_001199771.1:c.561C>T	NP_001186700.1:p.Asp187=
NM_002905.3:c.561C>T	NP_002896.2:p.Asp187=
NR_037658.1:n.620C>T
NM_001199771.2:c.561C>T	NP_001186700.1:p.Asp187=
NM_002905.5:c.561C>T MANE Select	NP_002896.2:p.Asp187=
NM_001199771.3:c.561C>T	NP_001186700.1:p.Asp187=