Canonical Allele Identifier: CA376359164
Community Standard Title: NM_014915.3(ANKRD26):c.4155T>G (p.His1385Gln)
Gene: ANKRD26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27022618A>C , CM000672.2:g.27022618A>C GRCh38
NC_000010.10:g.27311547A>C , CM000672.1:g.27311547A>C GRCh37
NC_000010.9:g.27351553A>C NCBI36
NG_031973.2:g.82881T>G , LRG_605:g.82881T>G

Transcript Alleles

HGVS Amino-acid Change
NM_014915.3:c.4155T>G MANE Select NP_055730.2:p.His1385Gln
ENST00000376087.5:c.4155T>G MANE Select ENSP00000365255.4:p.His1385Gln
NM_001256053.1:c.4152T>G NP_001242982.1:p.His1384Gln
NM_001256053.2:c.4152T>G NP_001242982.1:p.His1384Gln
NM_014915.2:c.4155T>G , LRG_605t1:c.4155T>G NP_055730.2:p.His1385Gln
ENST00000376087.4:c.4155T>G ENSP00000365255.4:p.His1385Gln
ENST00000436985.6:c.4203T>G ENSP00000405112.2:p.His1401Gln
ENST00000436985.7:c.4152T>G ENSP00000405112.3:p.His1384Gln
ENST00000675116.1:c.2013T>G
ENST00000675936.1:c.571T>G
XM_006717423.2:c.5241T>G XP_006717486.1:p.His1747Gln
XM_006717424.2:c.5238T>G XP_006717487.1:p.His1746Gln
XM_006717425.2:c.5241T>G XP_006717488.1:p.His1747Gln
XM_006717425.4:c.5241T>G XP_006717488.1:p.His1747Gln
XM_006717427.2:c.4398T>G XP_006717490.1:p.His1466Gln
XM_006717428.2:c.4056T>G XP_006717491.1:p.His1352Gln
XM_011519415.1:c.5229T>G XP_011517717.1:p.His1743Gln
XM_011519416.1:c.5241T>G XP_011517718.1:p.His1747Gln
XM_011519416.2:c.5241T>G XP_011517718.1:p.His1747Gln
XM_011519417.1:c.5241T>G XP_011517719.1:p.His1747Gln
XM_011519418.1:c.5241T>G XP_011517720.1:p.His1747Gln
XM_011519419.1:c.5142T>G XP_011517721.1:p.His1714Gln
XM_011519420.1:c.5241T>G XP_011517722.1:p.His1747Gln
XM_011519421.1:c.4398T>G XP_011517723.1:p.His1466Gln
XM_011519423.1:c.4398T>G XP_011517725.1:p.His1466Gln
XM_011519424.1:c.3855T>G XP_011517726.1:p.His1285Gln
XM_017015928.1:c.5241T>G XP_016871417.1:p.His1747Gln
XM_017015929.1:c.5229T>G XP_016871418.1:p.His1743Gln
XM_017015930.1:c.5241T>G XP_016871419.1:p.His1747Gln
XM_017015931.1:c.5241T>G XP_016871420.1:p.His1747Gln
XM_017015932.1:c.5241T>G XP_016871421.1:p.His1747Gln
XM_017015933.1:c.*478T>G XP_016871422.1:n.*478T>G
XR_930483.1:n.5413T>G
XR_930484.1:n.5413T>G