Canonical Allele Identifier: CA5447840

Gene: ANKRD26

Linked Data

• ClinVar Variation Id: 260469
• ClinVar RCV Id: RCV000242378 ; RCV000405230 ; RCV000901657
• dbSNP Id: rs78251061
• ExAC: 10:27311557 A / T
• gnomAD v2: 10-27311557-A-T
• gnomAD v3: 10-27022628-A-T
• gnomAD v4: 10-27022628-A-T
• MyVariant Identifiers: chr10:g.27311557A>T (hg19) ; chr10:g.27022628A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27022628A>T , CM000672.2:g.27022628A>T	GRCh38
NC_000010.10:g.27311557A>T , CM000672.1:g.27311557A>T	GRCh37
NC_000010.9:g.27351563A>T	NCBI36
NG_031973.2:g.82871T>A , LRG_605:g.82871T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376087.5:c.4145T>A MANE Select	ENSP00000365255.4:p.Phe1382Tyr
ENST00000436985.7:c.4142T>A	ENSP00000405112.3:p.Phe1381Tyr
ENST00000675116.1:c.2003T>A
ENST00000675936.1:c.561T>A
ENST00000376087.4:c.4145T>A	ENSP00000365255.4:p.Phe1382Tyr
ENST00000436985.6:c.4193T>A	ENSP00000405112.2:p.Phe1398Tyr
NM_001256053.1:c.4142T>A	NP_001242982.1:p.Phe1381Tyr
NM_014915.2:c.4145T>A , LRG_605t1:c.4145T>A	NP_055730.2:p.Phe1382Tyr
XM_006717423.2:c.5231T>A	XP_006717486.1:p.Phe1744Tyr
XM_006717424.2:c.5228T>A	XP_006717487.1:p.Phe1743Tyr
XM_006717425.2:c.5231T>A	XP_006717488.1:p.Phe1744Tyr
XM_006717427.2:c.4388T>A	XP_006717490.1:p.Phe1463Tyr
XM_006717428.2:c.4046T>A	XP_006717491.1:p.Phe1349Tyr
XM_011519415.1:c.5219T>A	XP_011517717.1:p.Phe1740Tyr
XM_011519416.1:c.5231T>A	XP_011517718.1:p.Phe1744Tyr
XM_011519417.1:c.5231T>A	XP_011517719.1:p.Phe1744Tyr
XM_011519418.1:c.5231T>A	XP_011517720.1:p.Phe1744Tyr
XM_011519419.1:c.5132T>A	XP_011517721.1:p.Phe1711Tyr
XM_011519420.1:c.5231T>A	XP_011517722.1:p.Phe1744Tyr
XM_011519421.1:c.4388T>A	XP_011517723.1:p.Phe1463Tyr
XM_011519423.1:c.4388T>A	XP_011517725.1:p.Phe1463Tyr
XM_011519424.1:c.3845T>A	XP_011517726.1:p.Phe1282Tyr
XR_930483.1:n.5403T>A
XR_930484.1:n.5403T>A
XM_006717425.4:c.5231T>A	XP_006717488.1:p.Phe1744Tyr
XM_011519416.2:c.5231T>A	XP_011517718.1:p.Phe1744Tyr
XM_017015928.1:c.5231T>A	XP_016871417.1:p.Phe1744Tyr
XM_017015929.1:c.5219T>A	XP_016871418.1:p.Phe1740Tyr
XM_017015930.1:c.5231T>A	XP_016871419.1:p.Phe1744Tyr
XM_017015931.1:c.5231T>A	XP_016871420.1:p.Phe1744Tyr
XM_017015932.1:c.5231T>A	XP_016871421.1:p.Phe1744Tyr
XM_017015933.1:c.*468T>A	XP_016871422.1:n.*468T>A
NM_001256053.2:c.4142T>A	NP_001242982.1:p.Phe1381Tyr
NM_014915.3:c.4145T>A MANE Select	NP_055730.2:p.Phe1382Tyr