Canonical Allele Identifier: CA376361023
Gene: ANKRD26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27033284T>G , CM000672.2:g.27033284T>G GRCh38
NC_000010.10:g.27322213T>G , CM000672.1:g.27322213T>G GRCh37
NC_000010.9:g.27362219T>G NCBI36
NG_031973.2:g.72215A>C , LRG_605:g.72215A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376087.5:c.3748A>C MANE Select ENSP00000365255.4:p.Ile1250Leu
ENST00000436985.7:c.3745A>C ENSP00000405112.3:p.Ile1249Leu
ENST00000675116.1:c.1398A>C
ENST00000675936.1:c.164A>C
ENST00000376087.4:c.3748A>C ENSP00000365255.4:p.Ile1250Leu
ENST00000436985.6:c.3796A>C ENSP00000405112.2:p.Ile1266Leu
NM_001256053.1:c.3745A>C NP_001242982.1:p.Ile1249Leu
NM_014915.2:c.3748A>C , LRG_605t1:c.3748A>C NP_055730.2:p.Ile1250Leu
XM_006717423.2:c.4834A>C XP_006717486.1:p.Ile1612Leu
XM_006717424.2:c.4831A>C XP_006717487.1:p.Ile1611Leu
XM_006717425.2:c.4834A>C XP_006717488.1:p.Ile1612Leu
XM_006717427.2:c.3991A>C XP_006717490.1:p.Ile1331Leu
XM_006717428.2:c.3649A>C XP_006717491.1:p.Ile1217Leu
XM_011519415.1:c.4822A>C XP_011517717.1:p.Ile1608Leu
XM_011519416.1:c.4834A>C XP_011517718.1:p.Ile1612Leu
XM_011519417.1:c.4834A>C XP_011517719.1:p.Ile1612Leu
XM_011519418.1:c.4834A>C XP_011517720.1:p.Ile1612Leu
XM_011519419.1:c.4735A>C XP_011517721.1:p.Ile1579Leu
XM_011519420.1:c.4834A>C XP_011517722.1:p.Ile1612Leu
XM_011519421.1:c.3991A>C XP_011517723.1:p.Ile1331Leu
XM_011519422.1:c.4834A>C XP_011517724.1:p.Ile1612Leu
XM_011519423.1:c.3991A>C XP_011517725.1:p.Ile1331Leu
XM_011519424.1:c.3448A>C XP_011517726.1:p.Ile1150Leu
XR_930483.1:n.5006A>C
XR_930484.1:n.5006A>C
XM_006717425.4:c.4834A>C XP_006717488.1:p.Ile1612Leu
XM_011519416.2:c.4834A>C XP_011517718.1:p.Ile1612Leu
XM_017015928.1:c.4834A>C XP_016871417.1:p.Ile1612Leu
XM_017015929.1:c.4822A>C XP_016871418.1:p.Ile1608Leu
XM_017015930.1:c.4834A>C XP_016871419.1:p.Ile1612Leu
XM_017015931.1:c.4834A>C XP_016871420.1:p.Ile1612Leu
XM_017015932.1:c.4834A>C XP_016871421.1:p.Ile1612Leu
XM_017015933.1:c.4834A>C XP_016871422.1:p.Ile1612Leu
NM_001256053.2:c.3745A>C NP_001242982.1:p.Ile1249Leu
NM_014915.3:c.3748A>C MANE Select NP_055730.2:p.Ile1250Leu