Canonical Allele Identifier: CA376361159

Gene: ANKRD26

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27033340G>C , CM000672.2:g.27033340G>C	GRCh38
NC_000010.10:g.27322269G>C , CM000672.1:g.27322269G>C	GRCh37
NC_000010.9:g.27362275G>C	NCBI36
NG_031973.2:g.72159C>G , LRG_605:g.72159C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014915.3:c.3692C>G MANE Select	NP_055730.2:p.Thr1231Ser
ENST00000376087.5:c.3692C>G MANE Select	ENSP00000365255.4:p.Thr1231Ser
NM_001256053.1:c.3689C>G	NP_001242982.1:p.Thr1230Ser
NM_001256053.2:c.3689C>G	NP_001242982.1:p.Thr1230Ser
NM_014915.2:c.3692C>G , LRG_605t1:c.3692C>G	NP_055730.2:p.Thr1231Ser
ENST00000376087.4:c.3692C>G	ENSP00000365255.4:p.Thr1231Ser
ENST00000436985.6:c.3740C>G	ENSP00000405112.2:p.Thr1247Ser
ENST00000436985.7:c.3689C>G	ENSP00000405112.3:p.Thr1230Ser
ENST00000675116.1:c.1342C>G
ENST00000675936.1:c.108C>G
XM_006717423.2:c.4778C>G	XP_006717486.1:p.Thr1593Ser
XM_006717424.2:c.4775C>G	XP_006717487.1:p.Thr1592Ser
XM_006717425.2:c.4778C>G	XP_006717488.1:p.Thr1593Ser
XM_006717425.4:c.4778C>G	XP_006717488.1:p.Thr1593Ser
XM_006717427.2:c.3935C>G	XP_006717490.1:p.Thr1312Ser
XM_006717428.2:c.3593C>G	XP_006717491.1:p.Thr1198Ser
XM_011519415.1:c.4766C>G	XP_011517717.1:p.Thr1589Ser
XM_011519416.1:c.4778C>G	XP_011517718.1:p.Thr1593Ser
XM_011519416.2:c.4778C>G	XP_011517718.1:p.Thr1593Ser
XM_011519417.1:c.4778C>G	XP_011517719.1:p.Thr1593Ser
XM_011519418.1:c.4778C>G	XP_011517720.1:p.Thr1593Ser
XM_011519419.1:c.4679C>G	XP_011517721.1:p.Thr1560Ser
XM_011519420.1:c.4778C>G	XP_011517722.1:p.Thr1593Ser
XM_011519421.1:c.3935C>G	XP_011517723.1:p.Thr1312Ser
XM_011519422.1:c.4778C>G	XP_011517724.1:p.Thr1593Ser
XM_011519423.1:c.3935C>G	XP_011517725.1:p.Thr1312Ser
XM_011519424.1:c.3392C>G	XP_011517726.1:p.Thr1131Ser
XM_011519425.1:c.*54C>G	XP_011517727.1:n.*54C>G
XM_017015928.1:c.4778C>G	XP_016871417.1:p.Thr1593Ser
XM_017015929.1:c.4766C>G	XP_016871418.1:p.Thr1589Ser
XM_017015930.1:c.4778C>G	XP_016871419.1:p.Thr1593Ser
XM_017015931.1:c.4778C>G	XP_016871420.1:p.Thr1593Ser
XM_017015932.1:c.4778C>G	XP_016871421.1:p.Thr1593Ser
XM_017015933.1:c.4778C>G	XP_016871422.1:p.Thr1593Ser
XR_930483.1:n.4950C>G
XR_930484.1:n.4950C>G