Canonical Allele Identifier: CA2740098017
Community Standard Title: NM_005989.4(AKR1D1):c.467_469dup (p.Ala156_Cys157insSer)
Gene: AKR1D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.138105317_138105319dup , CM000669.2:g.138105317_138105319dup GRCh38
NC_000007.13:g.137790063_137790065dup , CM000669.1:g.137790063_137790065dup GRCh37
NC_000007.12:g.137440603_137440605dup NCBI36
NG_023342.1:g.33886_33888dup

Transcript Alleles

HGVS Amino-acid Change
NM_005989.4:c.467_469dup MANE Select NP_005980.1:p.Ala156_Cys157insSer
ENST00000242375.8:c.467_469dup MANE Select ENSP00000242375.3:p.Ala156_Cys157insSer
NM_001190906.1:c.457-1291_457-1289dup NP_001177835.1:n.457-1291_457-1289dup
NM_001190906.2:c.457-1291_457-1289dup NP_001177835.1:n.457-1291_457-1289dup
NM_001190907.1:c.467_469dup NP_001177836.1:p.Ala156_Cys157insSer
NM_001190907.2:c.467_469dup NP_001177836.1:p.Ala156_Cys157insSer
NM_005989.3:c.467_469dup NP_005980.1:p.Ala156_Cys157insSer
ENST00000242375.7:c.467_469dup ENSP00000242375.3:p.Ala156_Cys157insSer
ENST00000411726.6:c.457-1291_457-1289dup ENSP00000402374.2:n.457-1291_457-1289dup
ENST00000432161.5:c.467_469dup ENSP00000389197.1:p.Ala156_Cys157insSer
ENST00000468877.2:n.377_379dup