Canonical Allele Identifier: CA1746468599

Gene: AKR1D1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138091753_138091755delinsCTT , CM000669.2:g.138091753_138091755delinsCTT	GRCh38
NC_000007.13:g.137776499_137776501delinsCTT , CM000669.1:g.137776499_137776501delinsCTT	GRCh37
NC_000007.12:g.137427039_137427041delinsCTT	NCBI36
NG_023342.1:g.20322_20324delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242375.8:c.262-15_262-13delinsCTT MANE Select	ENSP00000242375.3:n.262-15_262-13delinsCTT
ENST00000242375.7:c.262-15_262-13delinsCTT	ENSP00000242375.3:n.262-15_262-13delinsCTT
ENST00000411726.6:c.262-15_262-13delinsCTT	ENSP00000402374.2:n.262-15_262-13delinsCTT
ENST00000432161.5:c.262-15_262-13delinsCTT	ENSP00000389197.1:n.262-15_262-13delinsCTT
ENST00000438242.1:c.94-15_94-13delinsCTT	ENSP00000397042.1:n.94-15_94-13delinsCTT
ENST00000468877.2:n.222-65_222-63delinsCTT
NM_001190906.1:c.262-15_262-13delinsCTT	NP_001177835.1:n.262-15_262-13delinsCTT
NM_001190907.1:c.262-15_262-13delinsCTT	NP_001177836.1:n.262-15_262-13delinsCTT
NM_005989.3:c.262-15_262-13delinsCTT	NP_005980.1:n.262-15_262-13delinsCTT
NM_005989.4:c.262-15_262-13delinsCTT MANE Select	NP_005980.1:n.262-15_262-13delinsCTT
NM_001190906.2:c.262-15_262-13delinsCTT	NP_001177835.1:n.262-15_262-13delinsCTT
NM_001190907.2:c.262-15_262-13delinsCTT	NP_001177836.1:n.262-15_262-13delinsCTT