Canonical Allele Identifier: CA480360952

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115484C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721700C>T , CM000674.2:g.55721700C>T	GRCh38
NC_000012.11:g.56115484C>T , CM000674.1:g.56115484C>T	GRCh37
NC_000012.10:g.54401751C>T	NCBI36
NG_008606.1:g.6334C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.322C>T MANE Select	ENSP00000257895.6:p.Leu108=
ENST00000257895.9:c.322C>T	ENSP00000257895.5:p.Leu108=
ENST00000257899.3:c.337C>T
ENST00000547072.5:c.31C>T	ENSP00000449927.1:p.Leu11=
ENST00000547301.1:n.430C>T
ENST00000548082.1:c.322C>T	ENSP00000447128.1:p.Leu108=
ENST00000548123.1:c.300+206C>T
ENST00000548486.1:n.332C>T
ENST00000549424.1:c.129C>T	ENSP00000447621.1:p.Val43=
ENST00000550412.5:c.363C>T	ENSP00000447650.1:p.Val121=
ENST00000550608.1:n.461C>T
ENST00000551946.5:c.*125C>T	ENSP00000450201.1:n.*125C>T
ENST00000552930.5:c.31C>T	ENSP00000448014.1:p.Leu11=
ENST00000553160.1:n.406-495C>T
ENST00000553187.5:n.332C>T
NM_001199771.1:c.322C>T	NP_001186700.1:p.Leu108=
NM_002905.3:c.322C>T	NP_002896.2:p.Leu108=
NR_037658.1:n.381C>T
NM_001199771.2:c.322C>T	NP_001186700.1:p.Leu108=
NM_002905.5:c.322C>T MANE Select	NP_002896.2:p.Leu108=
NM_001199771.3:c.322C>T	NP_001186700.1:p.Leu108=