Canonical Allele Identifier: CA2038069414

Gene: RDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721711T= , CM000674.2:g.55721711T=	GRCh38
NC_000012.11:g.56115495T= , CM000674.1:g.56115495T=	GRCh37
NC_000012.10:g.54401762T=	NCBI36
NG_008606.1:g.6345T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257895.10:c.333T= MANE Select	ENSP00000257895.6:p.Asn111=
ENST00000257895.9:c.333T=	ENSP00000257895.5:p.Asn111=
ENST00000257899.3:c.348T=
ENST00000547072.5:c.42T=	ENSP00000449927.1:p.Asn14=
ENST00000547301.1:n.441T=
ENST00000548082.1:c.333T=	ENSP00000447128.1:p.Asn111=
ENST00000548123.1:c.300+217T=
ENST00000548486.1:n.343T=
ENST00000549424.1:c.*5T=	ENSP00000447621.1:n.*5T=
ENST00000550412.5:c.*5T=	ENSP00000447650.1:n.*5T=
ENST00000550608.1:n.472T=
ENST00000551946.5:c.*136T=	ENSP00000450201.1:n.*136T=
ENST00000552930.5:c.42T=	ENSP00000448014.1:p.Asn14=
ENST00000553160.1:n.406-484T=
ENST00000553187.5:n.343T=
NM_001199771.1:c.333T=	NP_001186700.1:p.Asn111=
NM_002905.3:c.333T=	NP_002896.2:p.Asn111=
NR_037658.1:n.392T=
NM_001199771.2:c.333T=	NP_001186700.1:p.Asn111=
NM_002905.5:c.333T= MANE Select	NP_002896.2:p.Asn111=
NM_001199771.3:c.333T=	NP_001186700.1:p.Asn111=