Canonical Allele Identifier: CA2685107402

Gene: AKR1D1

Linked Data

• gnomAD v4: 7-138091675-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138091675_138091676insC , CM000669.2:g.138091675_138091676insC	GRCh38
NC_000007.13:g.137776421_137776422insC , CM000669.1:g.137776421_137776422insC	GRCh37
NC_000007.12:g.137426961_137426962insC	NCBI36
NG_023342.1:g.20244_20245insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242375.8:c.262-93_262-92insC MANE Select	ENSP00000242375.3:n.262-93_262-92insC
ENST00000242375.7:c.262-93_262-92insC	ENSP00000242375.3:n.262-93_262-92insC
ENST00000411726.6:c.262-93_262-92insC	ENSP00000402374.2:n.262-93_262-92insC
ENST00000432161.5:c.262-93_262-92insC	ENSP00000389197.1:n.262-93_262-92insC
ENST00000438242.1:c.94-93_94-92insC	ENSP00000397042.1:n.94-93_94-92insC
ENST00000468877.2:n.222-143_222-142insC
NM_001190906.1:c.262-93_262-92insC	NP_001177835.1:n.262-93_262-92insC
NM_001190907.1:c.262-93_262-92insC	NP_001177836.1:n.262-93_262-92insC
NM_005989.3:c.262-93_262-92insC	NP_005980.1:n.262-93_262-92insC
NM_005989.4:c.262-93_262-92insC MANE Select	NP_005980.1:n.262-93_262-92insC
NM_001190906.2:c.262-93_262-92insC	NP_001177835.1:n.262-93_262-92insC
NM_001190907.2:c.262-93_262-92insC	NP_001177836.1:n.262-93_262-92insC