Canonical Allele Identifier: CA2608080766

Linked Data

gnomAD v4: 10-5099011-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.5099011G>T , CM000672.2:g.5099011G>T GRCh38
NC_000010.10:g.5141203G>T , CM000672.1:g.5141203G>T GRCh37
NC_000010.9:g.5131203G>T NCBI36
NG_047094.1:g.55246G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000380554.5:c.447+132G>T (AKR1C3) MANE Select ENSP00000369927.3:n.447+132G>T
ENST00000380554.4:c.447+132G>T (AKR1C3) ENSP00000369927.3:n.447+132G>T
ENST00000407674.5:c.180+33663C>A (AKR1C2) ENSP00000385221.2:n.180+33663C>A
ENST00000434459.6:c.933-8450G>T (AKR1C1) ENSP00000412248.3:n.933-8450G>T
ENST00000439082.7:c.447+132G>T ENSP00000401327.3:n.447+132G>T
ENST00000602997.5:c.378+132G>T (AKR1C3) ENSP00000474188.1:n.378+132G>T
ENST00000605149.5:c.378+132G>T (AKR1C3) ENSP00000474882.1:n.378+132G>T
ENST00000605322.1:n.280-316G>T (AKR1C3)
ENST00000605781.5:n.626+132G>T (AKR1C3)
NM_001253908.1:c.447+132G>T (AKR1C3) NP_001240837.1:n.447+132G>T
NM_003739.5:c.447+132G>T (AKR1C3) NP_003730.4:n.447+132G>T
NM_003739.6:c.447+132G>T (AKR1C3) MANE Select NP_003730.4:n.447+132G>T
NM_001253908.2:c.447+132G>T (AKR1C3) NP_001240837.1:n.447+132G>T