Canonical Allele Identifier: CA2796088836

Gene: RDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55722019_55722020insA , CM000674.2:g.55722019_55722020insA	GRCh38
NC_000012.11:g.56115803_56115804insA , CM000674.1:g.56115803_56115804insA	GRCh37
NC_000012.10:g.54402070_54402071insA	NCBI36
NG_008606.1:g.6653_6654insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.569+72_569+73insA MANE Select	ENSP00000257895.6:n.569+72_569+73insA
ENST00000257895.9:c.569+72_569+73insA	ENSP00000257895.5:n.569+72_569+73insA
ENST00000257899.3:c.591+65_591+66insA
ENST00000547072.5:c.278+72_278+73insA	ENSP00000449927.1:n.278+72_278+73insA
ENST00000548082.1:c.569+72_569+73insA	ENSP00000447128.1:n.569+72_569+73insA
ENST00000548123.1:c.300+525_300+526insA
ENST00000548486.1:n.651_652insA
ENST00000550412.5:c.*313_*314insA	ENSP00000447650.1:n.*313_*314insA
ENST00000550608.1:n.780_781insA
ENST00000551946.5:c.*444_*445insA	ENSP00000450201.1:n.*444_*445insA
ENST00000553160.1:n.406-176_406-175insA
NM_001199771.1:c.569+72_569+73insA	NP_001186700.1:n.569+72_569+73insA
NM_002905.3:c.569+72_569+73insA	NP_002896.2:n.569+72_569+73insA
NR_037658.1:n.628+72_628+73insA
NM_001199771.2:c.569+72_569+73insA	NP_001186700.1:n.569+72_569+73insA
NM_002905.5:c.569+72_569+73insA MANE Select	NP_002896.2:n.569+72_569+73insA
NM_001199771.3:c.569+72_569+73insA	NP_001186700.1:n.569+72_569+73insA