Canonical Allele Identifier: CA2580912164

Gene: AKR1E2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.4839654C>G , CM000672.2:g.4839654C>G	GRCh38
NC_000010.10:g.4881846C>G , CM000672.1:g.4881846C>G	GRCh37
NC_000010.9:g.4871846C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298375.12:c.583-75C>G MANE Select	ENSP00000298375.7:n.583-75C>G
ENST00000298375.11:c.583-75C>G	ENSP00000298375.7:n.583-75C>G
ENST00000334019.4:c.582+2073C>G	ENSP00000335034.4:n.582+2073C>G
ENST00000345253.9:c.460-2767C>G	ENSP00000335603.5:n.460-2767C>G
ENST00000441590.5:n.370+2073C>G
ENST00000462718.7:n.596-75C>G
ENST00000463345.5:c.583-75C>G	ENSP00000436794.1:n.583-75C>G
ENST00000474119.5:c.271-75C>G	ENSP00000434437.1:n.271-75C>G
ENST00000525281.5:n.535+2073C>G
ENST00000525572.1:c.336-75C>G
ENST00000532248.5:c.582+2073C>G	ENSP00000432947.1:n.582+2073C>G
NM_001040177.2:c.583-75C>G	NP_001035267.1:n.583-75C>G
NM_001271021.1:c.582+2073C>G	NP_001257950.1:n.582+2073C>G
NM_001271025.1:c.460-2767C>G	NP_001257954.1:n.460-2767C>G
NR_073125.1:n.731-75C>G
NR_073126.1:n.645-75C>G
NR_073127.1:n.730+2073C>G
XM_006717514.2:c.465+2073C>G	XP_006717577.1:n.465+2073C>G
XM_011519715.1:c.646-75C>G	XP_011518017.1:n.646-75C>G
XM_011519716.1:c.646-75C>G	XP_011518018.1:n.646-75C>G
XM_011519717.1:c.529-75C>G	XP_011518019.1:n.529-75C>G
XM_011519718.1:c.646-75C>G	XP_011518020.1:n.646-75C>G
XM_011519719.1:c.646-75C>G	XP_011518021.1:n.646-75C>G
XM_011519720.1:c.646-75C>G	XP_011518022.1:n.646-75C>G
XM_011519721.1:c.646-75C>G	XP_011518023.1:n.646-75C>G
XM_011519722.1:c.646-75C>G	XP_011518024.1:n.646-75C>G
XM_011519723.1:c.646-75C>G	XP_011518025.1:n.646-75C>G
XM_011519724.1:c.645+2073C>G	XP_011518026.1:n.645+2073C>G
XM_011519725.1:c.646-75C>G	XP_011518027.1:n.646-75C>G
XM_011519726.1:c.523-2767C>G	XP_011518028.1:n.523-2767C>G
XM_011519727.1:c.465+2073C>G	XP_011518029.1:n.465+2073C>G
XM_011519728.1:c.271-75C>G	XP_011518030.1:n.271-75C>G
XM_011519729.1:c.645+2073C>G	XP_011518031.1:n.645+2073C>G
XR_930518.1:n.1018-75C>G
XR_930519.1:n.1019-75C>G
XR_930520.1:n.1018-75C>G
XM_011519715.2:c.646-75C>G	XP_011518017.1:n.646-75C>G
XM_011519718.2:c.646-75C>G	XP_011518020.1:n.646-75C>G
XM_011519719.2:c.646-75C>G	XP_011518021.1:n.646-75C>G
XM_011519720.2:c.646-75C>G	XP_011518022.1:n.646-75C>G
XM_011519722.2:c.646-75C>G	XP_011518024.1:n.646-75C>G
XM_011519724.2:c.645+2073C>G	XP_011518026.1:n.645+2073C>G
XM_011519725.2:c.646-75C>G	XP_011518027.1:n.646-75C>G
XM_017016743.1:c.646-75C>G	XP_016872232.1:n.646-75C>G
XM_017016744.1:c.646-75C>G	XP_016872233.1:n.646-75C>G
XM_017016745.1:c.271-75C>G	XP_016872234.1:n.271-75C>G
XM_024448224.1:c.466-75C>G	XP_024303992.1:n.466-75C>G
XM_024448225.1:c.583-75C>G	XP_024303993.1:n.583-75C>G
XM_024448226.1:c.523-2767C>G	XP_024303994.1:n.523-2767C>G
XR_001747220.1:n.1028-75C>G
XR_001747221.1:n.698-75C>G
XR_001747222.1:n.1028-75C>G
XR_001747223.1:n.1743+2073C>G
XR_002957024.1:n.1024+2073C>G
XR_930518.2:n.1027-75C>G
XR_930519.2:n.1028-75C>G
XR_930520.2:n.1027-75C>G
NM_001040177.3:c.583-75C>G MANE Select	NP_001035267.1:n.583-75C>G
NM_001271021.2:c.582+2073C>G	NP_001257950.1:n.582+2073C>G
NM_001271025.2:c.460-2767C>G	NP_001257954.1:n.460-2767C>G
NR_073125.2:n.701-75C>G
NR_073127.2:n.700+2073C>G