Canonical Allele Identifier: CA2608080736

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5098968_5098970dup , CM000672.2:g.5098968_5098970dup GRCh38
NC_000010.10:g.5141160_5141162dup , CM000672.1:g.5141160_5141162dup GRCh37
NC_000010.9:g.5131160_5131162dup NCBI36
NG_047094.1:g.55203_55205dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+89_447+91dup (AKR1C3) MANE Select ENSP00000369927.3:n.447+89_447+91dup
ENST00000380554.4:c.447+89_447+91dup (AKR1C3) ENSP00000369927.3:n.447+89_447+91dup
ENST00000407674.5:c.180+33706_180+33708dup (AKR1C2) ENSP00000385221.2:n.180+33706_180+33708dup
ENST00000434459.6:c.933-8493_933-8491dup (AKR1C1) ENSP00000412248.3:n.933-8493_933-8491dup
ENST00000439082.7:c.447+89_447+91dup ENSP00000401327.3:n.447+89_447+91dup
ENST00000602997.5:c.378+89_378+91dup (AKR1C3) ENSP00000474188.1:n.378+89_378+91dup
ENST00000605149.5:c.378+89_378+91dup (AKR1C3) ENSP00000474882.1:n.378+89_378+91dup
ENST00000605322.1:n.280-359_280-357dup (AKR1C3)
ENST00000605781.5:n.626+89_626+91dup (AKR1C3)
NM_001253908.1:c.447+89_447+91dup (AKR1C3) NP_001240837.1:n.447+89_447+91dup
NM_003739.5:c.447+89_447+91dup (AKR1C3) NP_003730.4:n.447+89_447+91dup
NM_003739.6:c.447+89_447+91dup (AKR1C3) MANE Select NP_003730.4:n.447+89_447+91dup
NM_001253908.2:c.447+89_447+91dup (AKR1C3) NP_001240837.1:n.447+89_447+91dup