Canonical Allele Identifier: CA6616811

Gene: RDH5

Linked Data

• dbSNP Id: rs764628390
• ExAC: 12:56115500 G / T
• gnomAD v2: 12-56115500-G-T
• gnomAD v3: 12-55721716-G-T
• gnomAD v4: 12-55721716-G-T
• MyVariant Identifiers: chr12:g.56115500G>T (hg19) ; chr12:g.55721716G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721716G>T , CM000674.2:g.55721716G>T	GRCh38
NC_000012.11:g.56115500G>T , CM000674.1:g.56115500G>T	GRCh37
NC_000012.10:g.54401767G>T	NCBI36
NG_008606.1:g.6350G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.338G>T MANE Select	ENSP00000257895.6:p.Gly113Val
ENST00000257895.9:c.338G>T	ENSP00000257895.5:p.Gly113Val
ENST00000257899.3:c.353G>T
ENST00000547072.5:c.47G>T	ENSP00000449927.1:p.Gly16Val
ENST00000547301.1:n.446G>T
ENST00000548082.1:c.338G>T	ENSP00000447128.1:p.Gly113Val
ENST00000548123.1:c.300+222G>T
ENST00000548486.1:n.348G>T
ENST00000549424.1:c.*10G>T	ENSP00000447621.1:n.*10G>T
ENST00000550412.5:c.*10G>T	ENSP00000447650.1:n.*10G>T
ENST00000550608.1:n.477G>T
ENST00000551946.5:c.*141G>T	ENSP00000450201.1:n.*141G>T
ENST00000552930.5:c.47G>T	ENSP00000448014.1:p.Gly16Val
ENST00000553160.1:n.406-479G>T
ENST00000553187.5:n.348G>T
NM_001199771.1:c.338G>T	NP_001186700.1:p.Gly113Val
NM_002905.3:c.338G>T	NP_002896.2:p.Gly113Val
NR_037658.1:n.397G>T
NM_001199771.2:c.338G>T	NP_001186700.1:p.Gly113Val
NM_002905.5:c.338G>T MANE Select	NP_002896.2:p.Gly113Val
NM_001199771.3:c.338G>T	NP_001186700.1:p.Gly113Val