Canonical Allele Identifier: CA1887558029

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5099027_5099029delinsAAC , CM000672.2:g.5099027_5099029delinsAAC GRCh38
NC_000010.10:g.5141219_5141221delinsAAC , CM000672.1:g.5141219_5141221delinsAAC GRCh37
NC_000010.9:g.5131219_5131221delinsAAC NCBI36
NG_047094.1:g.55262_55264delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+148_447+150delinsAAC (AKR1C3) MANE Select ENSP00000369927.3:n.447+148_447+150delinsAAC
ENST00000380554.4:c.447+148_447+150delinsAAC (AKR1C3) ENSP00000369927.3:n.447+148_447+150delinsAAC
ENST00000407674.5:c.180+33645_180+33647delinsGTT (AKR1C2) ENSP00000385221.2:n.180+33645_180+33647delinsGTT
ENST00000434459.6:c.933-8434_933-8432delinsAAC (AKR1C1) ENSP00000412248.3:n.933-8434_933-8432delinsAAC
ENST00000439082.7:c.447+148_447+150delinsAAC ENSP00000401327.3:n.447+148_447+150delinsAAC
ENST00000602997.5:c.378+148_378+150delinsAAC (AKR1C3) ENSP00000474188.1:n.378+148_378+150delinsAAC
ENST00000605149.5:c.378+148_378+150delinsAAC (AKR1C3) ENSP00000474882.1:n.378+148_378+150delinsAAC
ENST00000605322.1:n.280-300_280-298delinsAAC (AKR1C3)
ENST00000605781.5:n.626+148_626+150delinsAAC (AKR1C3)
NM_001253908.1:c.447+148_447+150delinsAAC (AKR1C3) NP_001240837.1:n.447+148_447+150delinsAAC
NM_003739.5:c.447+148_447+150delinsAAC (AKR1C3) NP_003730.4:n.447+148_447+150delinsAAC
NM_003739.6:c.447+148_447+150delinsAAC (AKR1C3) MANE Select NP_003730.4:n.447+148_447+150delinsAAC
NM_001253908.2:c.447+148_447+150delinsAAC (AKR1C3) NP_001240837.1:n.447+148_447+150delinsAAC