Canonical Allele Identifier: CA385201235

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115722A>C (hg19) ; chr12:g.55721938A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721938A>C , CM000674.2:g.55721938A>C	GRCh38
NC_000012.11:g.56115722A>C , CM000674.1:g.56115722A>C	GRCh37
NC_000012.10:g.54401989A>C	NCBI36
NG_008606.1:g.6572A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.560A>C MANE Select	ENSP00000257895.6:p.Asp187Ala
ENST00000257895.9:c.560A>C	ENSP00000257895.5:p.Asp187Ala
ENST00000257899.3:c.575A>C
ENST00000547072.5:c.269A>C	ENSP00000449927.1:p.Asp90Ala
ENST00000548082.1:c.560A>C	ENSP00000447128.1:p.Asp187Ala
ENST00000548123.1:c.300+444A>C
ENST00000548486.1:n.570A>C
ENST00000550412.5:c.*232A>C	ENSP00000447650.1:n.*232A>C
ENST00000550608.1:n.699A>C
ENST00000551946.5:c.*363A>C	ENSP00000450201.1:n.*363A>C
ENST00000553160.1:n.406-257A>C
ENST00000553187.5:n.570A>C
NM_001199771.1:c.560A>C	NP_001186700.1:p.Asp187Ala
NM_002905.3:c.560A>C	NP_002896.2:p.Asp187Ala
NR_037658.1:n.619A>C
NM_001199771.2:c.560A>C	NP_001186700.1:p.Asp187Ala
NM_002905.5:c.560A>C MANE Select	NP_002896.2:p.Asp187Ala
NM_001199771.3:c.560A>C	NP_001186700.1:p.Asp187Ala