Canonical Allele Identifier: CA385201176

Gene: RDH5

Linked Data

• gnomAD v4: 12-55721920-G-A
• MyVariant Identifiers: chr12:g.56115704G>A (hg19) ; chr12:g.55721920G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721920G>A , CM000674.2:g.55721920G>A	GRCh38
NC_000012.11:g.56115704G>A , CM000674.1:g.56115704G>A	GRCh37
NC_000012.10:g.54401971G>A	NCBI36
NG_008606.1:g.6554G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257895.10:c.542G>A MANE Select	ENSP00000257895.6:p.Gly181Asp
ENST00000257895.9:c.542G>A	ENSP00000257895.5:p.Gly181Asp
ENST00000257899.3:c.557G>A
ENST00000547072.5:c.251G>A	ENSP00000449927.1:p.Gly84Asp
ENST00000548082.1:c.542G>A	ENSP00000447128.1:p.Gly181Asp
ENST00000548123.1:c.300+426G>A
ENST00000548486.1:n.552G>A
ENST00000550412.5:c.*214G>A	ENSP00000447650.1:n.*214G>A
ENST00000550608.1:n.681G>A
ENST00000551946.5:c.*345G>A	ENSP00000450201.1:n.*345G>A
ENST00000553160.1:n.406-275G>A
ENST00000553187.5:n.552G>A
NM_001199771.1:c.542G>A	NP_001186700.1:p.Gly181Asp
NM_002905.3:c.542G>A	NP_002896.2:p.Gly181Asp
NR_037658.1:n.601G>A
NM_001199771.2:c.542G>A	NP_001186700.1:p.Gly181Asp
NM_002905.5:c.542G>A MANE Select	NP_002896.2:p.Gly181Asp
NM_001199771.3:c.542G>A	NP_001186700.1:p.Gly181Asp