Canonical Allele Identifier: CA385201002

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115646A>T (hg19) ; chr12:g.55721862A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721862A>T , CM000674.2:g.55721862A>T	GRCh38
NC_000012.11:g.56115646A>T , CM000674.1:g.56115646A>T	GRCh37
NC_000012.10:g.54401913A>T	NCBI36
NG_008606.1:g.6496A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.484A>T MANE Select	ENSP00000257895.6:p.Thr162Ser
ENST00000257895.9:c.484A>T	ENSP00000257895.5:p.Thr162Ser
ENST00000257899.3:c.499A>T
ENST00000547072.5:c.193A>T	ENSP00000449927.1:p.Thr65Ser
ENST00000548082.1:c.484A>T	ENSP00000447128.1:p.Thr162Ser
ENST00000548123.1:c.300+368A>T
ENST00000548486.1:n.494A>T
ENST00000550412.5:c.*156A>T	ENSP00000447650.1:n.*156A>T
ENST00000550608.1:n.623A>T
ENST00000551946.5:c.*287A>T	ENSP00000450201.1:n.*287A>T
ENST00000553160.1:n.406-333A>T
ENST00000553187.5:n.494A>T
NM_001199771.1:c.484A>T	NP_001186700.1:p.Thr162Ser
NM_002905.3:c.484A>T	NP_002896.2:p.Thr162Ser
NR_037658.1:n.543A>T
NM_001199771.2:c.484A>T	NP_001186700.1:p.Thr162Ser
NM_002905.5:c.484A>T MANE Select	NP_002896.2:p.Thr162Ser
NM_001199771.3:c.484A>T	NP_001186700.1:p.Thr162Ser