Canonical Allele Identifier: CA2564061348

Gene: AKR1E2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.4847051T>C , CM000672.2:g.4847051T>C	GRCh38
NC_000010.10:g.4889243T>C , CM000672.1:g.4889243T>C	GRCh37
NC_000010.9:g.4879243T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298375.12:c.838-97T>C MANE Select	ENSP00000298375.7:n.838-97T>C
ENST00000298375.11:c.838-97T>C	ENSP00000298375.7:n.838-97T>C
ENST00000334019.4:c.667-97T>C	ENSP00000335034.4:n.667-97T>C
ENST00000345253.9:c.544-97T>C	ENSP00000335603.5:n.544-97T>C
ENST00000463345.5:c.838-97T>C	ENSP00000436794.1:n.838-97T>C
ENST00000474119.5:c.526-97T>C	ENSP00000434437.1:n.526-97T>C
ENST00000487985.1:c.184-97T>C
ENST00000532248.5:c.667-97T>C	ENSP00000432947.1:n.667-97T>C
NM_001040177.2:c.838-97T>C	NP_001035267.1:n.838-97T>C
NM_001271021.1:c.667-97T>C	NP_001257950.1:n.667-97T>C
NM_001271025.1:c.544-97T>C	NP_001257954.1:n.544-97T>C
NR_073125.1:n.986-97T>C
NR_073126.1:n.900-97T>C
NR_073127.1:n.815-97T>C
XM_011519715.1:c.901-97T>C	XP_011518017.1:n.901-97T>C
XM_011519717.1:c.784-97T>C	XP_011518019.1:n.784-97T>C
XM_011519718.1:c.901-437T>C	XP_011518020.1:n.901-437T>C
XM_011519720.1:c.*14-97T>C	XP_011518022.1:n.*14-97T>C
XM_011519722.1:c.*14-437T>C	XP_011518024.1:n.*14-437T>C
XM_011519723.1:c.*13+4547T>C	XP_011518025.1:n.*13+4547T>C
XM_011519724.1:c.730-97T>C	XP_011518026.1:n.730-97T>C
XM_011519726.1:c.607-97T>C	XP_011518028.1:n.607-97T>C
XM_011519727.1:c.550-97T>C	XP_011518029.1:n.550-97T>C
XM_011519728.1:c.526-97T>C	XP_011518030.1:n.526-97T>C
XR_930518.1:n.1273-97T>C
XR_930519.1:n.1393-97T>C
XR_930520.1:n.1256-97T>C
XM_011519715.2:c.901-97T>C	XP_011518017.1:n.901-97T>C
XM_011519718.2:c.901-437T>C	XP_011518020.1:n.901-437T>C
XM_011519720.2:c.*14-97T>C	XP_011518022.1:n.*14-97T>C
XM_011519722.2:c.*14-437T>C	XP_011518024.1:n.*14-437T>C
XM_011519724.2:c.730-97T>C	XP_011518026.1:n.730-97T>C
XM_017016744.1:c.*13+4547T>C	XP_016872233.1:n.*13+4547T>C
XM_017016745.1:c.526-437T>C	XP_016872234.1:n.526-437T>C
XM_024448224.1:c.721-97T>C	XP_024303992.1:n.721-97T>C
XM_024448225.1:c.838-437T>C	XP_024303993.1:n.838-437T>C
XM_024448226.1:c.607-437T>C	XP_024303994.1:n.607-437T>C
XR_001747220.1:n.1283-97T>C
XR_001747221.1:n.1072-97T>C
XR_001747222.1:n.1385-97T>C
XR_001747223.1:n.1947-97T>C
XR_002957024.1:n.1182-97T>C
XR_930518.2:n.1282-97T>C
XR_930519.2:n.1402-97T>C
XR_930520.2:n.1265-97T>C
NM_001040177.3:c.838-97T>C MANE Select	NP_001035267.1:n.838-97T>C
NM_001271021.2:c.667-97T>C	NP_001257950.1:n.667-97T>C
NM_001271025.2:c.544-97T>C	NP_001257954.1:n.544-97T>C
NR_073125.2:n.956-97T>C
NR_073127.2:n.785-97T>C