Canonical Allele Identifier: CA376361160

Gene: ANKRD26

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27033341T>A , CM000672.2:g.27033341T>A	GRCh38
NC_000010.10:g.27322270T>A , CM000672.1:g.27322270T>A	GRCh37
NC_000010.9:g.27362276T>A	NCBI36
NG_031973.2:g.72158A>T , LRG_605:g.72158A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014915.3:c.3691A>T MANE Select	NP_055730.2:p.Thr1231Ser
ENST00000376087.5:c.3691A>T MANE Select	ENSP00000365255.4:p.Thr1231Ser
NM_001256053.1:c.3688A>T	NP_001242982.1:p.Thr1230Ser
NM_001256053.2:c.3688A>T	NP_001242982.1:p.Thr1230Ser
NM_014915.2:c.3691A>T , LRG_605t1:c.3691A>T	NP_055730.2:p.Thr1231Ser
ENST00000376087.4:c.3691A>T	ENSP00000365255.4:p.Thr1231Ser
ENST00000436985.6:c.3739A>T	ENSP00000405112.2:p.Thr1247Ser
ENST00000436985.7:c.3688A>T	ENSP00000405112.3:p.Thr1230Ser
ENST00000675116.1:c.1341A>T
ENST00000675936.1:c.107A>T
XM_006717423.2:c.4777A>T	XP_006717486.1:p.Thr1593Ser
XM_006717424.2:c.4774A>T	XP_006717487.1:p.Thr1592Ser
XM_006717425.2:c.4777A>T	XP_006717488.1:p.Thr1593Ser
XM_006717425.4:c.4777A>T	XP_006717488.1:p.Thr1593Ser
XM_006717427.2:c.3934A>T	XP_006717490.1:p.Thr1312Ser
XM_006717428.2:c.3592A>T	XP_006717491.1:p.Thr1198Ser
XM_011519415.1:c.4765A>T	XP_011517717.1:p.Thr1589Ser
XM_011519416.1:c.4777A>T	XP_011517718.1:p.Thr1593Ser
XM_011519416.2:c.4777A>T	XP_011517718.1:p.Thr1593Ser
XM_011519417.1:c.4777A>T	XP_011517719.1:p.Thr1593Ser
XM_011519418.1:c.4777A>T	XP_011517720.1:p.Thr1593Ser
XM_011519419.1:c.4678A>T	XP_011517721.1:p.Thr1560Ser
XM_011519420.1:c.4777A>T	XP_011517722.1:p.Thr1593Ser
XM_011519421.1:c.3934A>T	XP_011517723.1:p.Thr1312Ser
XM_011519422.1:c.4777A>T	XP_011517724.1:p.Thr1593Ser
XM_011519423.1:c.3934A>T	XP_011517725.1:p.Thr1312Ser
XM_011519424.1:c.3391A>T	XP_011517726.1:p.Thr1131Ser
XM_011519425.1:c.*53A>T	XP_011517727.1:n.*53A>T
XM_017015928.1:c.4777A>T	XP_016871417.1:p.Thr1593Ser
XM_017015929.1:c.4765A>T	XP_016871418.1:p.Thr1589Ser
XM_017015930.1:c.4777A>T	XP_016871419.1:p.Thr1593Ser
XM_017015931.1:c.4777A>T	XP_016871420.1:p.Thr1593Ser
XM_017015932.1:c.4777A>T	XP_016871421.1:p.Thr1593Ser
XM_017015933.1:c.4777A>T	XP_016871422.1:p.Thr1593Ser
XR_930483.1:n.4949A>T
XR_930484.1:n.4949A>T