Canonical Allele Identifier: CA2786486524

Gene: AKR1C3 AKR1C2 AKR1C1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.5099026_5099027insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC , CM000672.2:g.5099026_5099027insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC	GRCh38
NC_000010.10:g.5141218_5141219insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC , CM000672.1:g.5141218_5141219insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC	GRCh37
NC_000010.9:g.5131218_5131219insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC	NCBI36
NG_047094.1:g.55261_55262insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380554.5:c.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C3) MANE Select	ENSP00000369927.3:n.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGG...
ENST00000380554.4:c.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C3)	ENSP00000369927.3:n.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGG...
ENST00000407674.5:c.180+33647_180+33648insGATGAGCGGTGTCCCTCGCAGCCATCTCGTCACGGGGATCGGGCTAGGCGATATCCGGGGAATAAAGCACGCCTACCTGCAGGCGCCCCACATAGCGC (AKR1C2)	ENSP00000385221.2:n.180+33647_180+33648insGATGAGCGGTGTCCCTCGC...
ENST00000434459.6:c.933-8435_933-8434insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C1)	ENSP00000412248.3:n.933-8435_933-8434insGCGCTATGTGGGGCGCCTGCA...
ENST00000439082.7:c.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC	ENSP00000401327.3:n.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGG...
ENST00000602997.5:c.378+147_378+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C3)	ENSP00000474188.1:n.378+147_378+148insGCGCTATGTGGGGCGCCTGCAGG...
ENST00000605149.5:c.378+147_378+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C3)	ENSP00000474882.1:n.378+147_378+148insGCGCTATGTGGGGCGCCTGCAGG...
ENST00000605322.1:n.280-301_280-300insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C3)
ENST00000605781.5:n.626+147_626+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C3)
NM_001253908.1:c.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C3)	NP_001240837.1:n.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAG...
NM_003739.5:c.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C3)	NP_003730.4:n.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCG...
NM_003739.6:c.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C3) MANE Select	NP_003730.4:n.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCG...
NM_001253908.2:c.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAGGCGTGCTTTATTCCCCGGATATCGCCTAGCCCGATCCCCGTGACGAGATGGCTGCGAGGGACACCGCTCATC (AKR1C3)	NP_001240837.1:n.447+147_447+148insGCGCTATGTGGGGCGCCTGCAGGTAG...