Canonical Allele Identifier: CA376352611

Gene: ANKRD26

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27005616C>T , CM000672.2:g.27005616C>T	GRCh38
NC_000010.10:g.27294545C>T , CM000672.1:g.27294545C>T	GRCh37
NC_000010.9:g.27334551C>T	NCBI36
NG_031973.2:g.99883G>A , LRG_605:g.99883G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014915.3:c.5107G>A MANE Select	NP_055730.2:p.Val1703Ile
ENST00000376087.5:c.5107G>A MANE Select	ENSP00000365255.4:p.Val1703Ile
NM_001256053.1:c.5104G>A	NP_001242982.1:p.Val1702Ile
NM_001256053.2:c.5104G>A	NP_001242982.1:p.Val1702Ile
NM_014915.2:c.5107G>A , LRG_605t1:c.5107G>A	NP_055730.2:p.Val1703Ile
ENST00000376087.4:c.5107G>A	ENSP00000365255.4:p.Val1703Ile
ENST00000436985.6:c.5155G>A	ENSP00000405112.2:p.Val1719Ile
ENST00000436985.7:c.5104G>A	ENSP00000405112.3:p.Val1702Ile
ENST00000445828.5:c.562+7G>A
ENST00000674670.1:c.489+1301G>A
ENST00000675116.1:c.2965G>A
ENST00000675439.1:c.324+1301G>A
ENST00000675936.1:c.1522+1G>A
ENST00000676280.1:c.489G>A
XM_006717423.2:c.6193G>A	XP_006717486.1:p.Val2065Ile
XM_006717424.2:c.6190G>A	XP_006717487.1:p.Val2064Ile
XM_006717425.2:c.6085+1301G>A	XP_006717488.1:n.6085+1301G>A
XM_006717425.4:c.6085+1301G>A	XP_006717488.1:n.6085+1301G>A
XM_006717427.2:c.5350G>A	XP_006717490.1:p.Val1784Ile
XM_006717428.2:c.5008G>A	XP_006717491.1:p.Val1670Ile
XM_011519415.1:c.6181G>A	XP_011517717.1:p.Val2061Ile
XM_011519416.1:c.6085+1301G>A	XP_011517718.1:n.6085+1301G>A
XM_011519416.2:c.6085+1301G>A	XP_011517718.1:n.6085+1301G>A
XM_011519417.1:c.6085+1301G>A	XP_011517719.1:n.6085+1301G>A
XM_011519418.1:c.6085+1301G>A	XP_011517720.1:n.6085+1301G>A
XM_011519419.1:c.6094G>A	XP_011517721.1:p.Val2032Ile
XM_011519420.1:c.5902G>A	XP_011517722.1:p.Val1968Ile
XM_011519421.1:c.5350G>A	XP_011517723.1:p.Val1784Ile
XM_011519423.1:c.5350G>A	XP_011517725.1:p.Val1784Ile
XM_011519424.1:c.4807G>A	XP_011517726.1:p.Val1603Ile
XM_017015928.1:c.6085+1301G>A	XP_016871417.1:n.6085+1301G>A
XM_017015929.1:c.6073+1301G>A	XP_016871418.1:n.6073+1301G>A
XM_017015930.1:c.6085+1301G>A	XP_016871419.1:n.6085+1301G>A
XM_017015931.1:c.6085+1301G>A	XP_016871420.1:n.6085+1301G>A
XM_017015932.1:c.6085+1301G>A	XP_016871421.1:n.6085+1301G>A
XM_017015933.1:c.*1430G>A	XP_016871422.1:n.*1430G>A
XR_930483.1:n.6257+1301G>A
XR_930484.1:n.6257+1301G>A