Canonical Allele Identifier: CA204420844

Gene: ANKRD26

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27060414T>C , CM000672.2:g.27060414T>C	GRCh38
NC_000010.10:g.27349343T>C , CM000672.1:g.27349343T>C	GRCh37
NC_000010.9:g.27389349T>C	NCBI36
NG_031973.2:g.45085A>G , LRG_605:g.45085A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014915.3:c.1495A>G MANE Select	NP_055730.2:p.Thr499Ala
ENST00000376087.5:c.1495A>G MANE Select	ENSP00000365255.4:p.Thr499Ala
NM_001256053.1:c.1495A>G	NP_001242982.1:p.Thr499Ala
NM_001256053.2:c.1495A>G	NP_001242982.1:p.Thr499Ala
NM_014915.2:c.1495A>G , LRG_605t1:c.1495A>G	NP_055730.2:p.Thr499Ala
ENST00000376087.4:c.1495A>G	ENSP00000365255.4:p.Thr499Ala
ENST00000436985.6:c.1543A>G	ENSP00000405112.2:p.Thr515Ala
ENST00000436985.7:c.1495A>G	ENSP00000405112.3:p.Thr499Ala
ENST00000675187.1:c.*834A>G	ENSP00000502611.1:n.*834A>G
ENST00000675846.1:c.1401A>G
ENST00000676232.1:c.1203A>G
ENST00000676420.1:c.*1315A>G	ENSP00000502355.1:n.*1315A>G
XM_006717423.2:c.1495A>G	XP_006717486.1:p.Thr499Ala
XM_006717424.2:c.1495A>G	XP_006717487.1:p.Thr499Ala
XM_006717425.2:c.1495A>G	XP_006717488.1:p.Thr499Ala
XM_006717425.4:c.1495A>G	XP_006717488.1:p.Thr499Ala
XM_006717427.2:c.652A>G	XP_006717490.1:p.Thr218Ala
XM_006717428.2:c.1396A>G	XP_006717491.1:p.Thr466Ala
XM_011519415.1:c.1483A>G	XP_011517717.1:p.Thr495Ala
XM_011519416.1:c.1495A>G	XP_011517718.1:p.Thr499Ala
XM_011519416.2:c.1495A>G	XP_011517718.1:p.Thr499Ala
XM_011519417.1:c.1495A>G	XP_011517719.1:p.Thr499Ala
XM_011519418.1:c.1495A>G	XP_011517720.1:p.Thr499Ala
XM_011519419.1:c.1396A>G	XP_011517721.1:p.Thr466Ala
XM_011519420.1:c.1495A>G	XP_011517722.1:p.Thr499Ala
XM_011519421.1:c.652A>G	XP_011517723.1:p.Thr218Ala
XM_011519422.1:c.1495A>G	XP_011517724.1:p.Thr499Ala
XM_011519423.1:c.652A>G	XP_011517725.1:p.Thr218Ala
XM_011519424.1:c.109A>G	XP_011517726.1:p.Thr37Ala
XM_011519425.1:c.1495A>G	XP_011517727.1:p.Thr499Ala
XM_017015928.1:c.1495A>G	XP_016871417.1:p.Thr499Ala
XM_017015929.1:c.1483A>G	XP_016871418.1:p.Thr495Ala
XM_017015930.1:c.1495A>G	XP_016871419.1:p.Thr499Ala
XM_017015931.1:c.1495A>G	XP_016871420.1:p.Thr499Ala
XM_017015932.1:c.1495A>G	XP_016871421.1:p.Thr499Ala
XM_017015933.1:c.1495A>G	XP_016871422.1:p.Thr499Ala
XM_024447896.1:c.1495A>G	XP_024303664.1:p.Thr499Ala
XR_930483.1:n.1667A>G
XR_930484.1:n.1667A>G