Canonical Allele Identifier: CA376361032
Gene: ANKRD26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27033289T>A , CM000672.2:g.27033289T>A GRCh38
NC_000010.10:g.27322218T>A , CM000672.1:g.27322218T>A GRCh37
NC_000010.9:g.27362224T>A NCBI36
NG_031973.2:g.72210A>T , LRG_605:g.72210A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376087.5:c.3743A>T MANE Select ENSP00000365255.4:p.Tyr1248Phe
ENST00000436985.7:c.3740A>T ENSP00000405112.3:p.Tyr1247Phe
ENST00000675116.1:c.1393A>T
ENST00000675936.1:c.159A>T
ENST00000376087.4:c.3743A>T ENSP00000365255.4:p.Tyr1248Phe
ENST00000436985.6:c.3791A>T ENSP00000405112.2:p.Tyr1264Phe
NM_001256053.1:c.3740A>T NP_001242982.1:p.Tyr1247Phe
NM_014915.2:c.3743A>T , LRG_605t1:c.3743A>T NP_055730.2:p.Tyr1248Phe
XM_006717423.2:c.4829A>T XP_006717486.1:p.Tyr1610Phe
XM_006717424.2:c.4826A>T XP_006717487.1:p.Tyr1609Phe
XM_006717425.2:c.4829A>T XP_006717488.1:p.Tyr1610Phe
XM_006717427.2:c.3986A>T XP_006717490.1:p.Tyr1329Phe
XM_006717428.2:c.3644A>T XP_006717491.1:p.Tyr1215Phe
XM_011519415.1:c.4817A>T XP_011517717.1:p.Tyr1606Phe
XM_011519416.1:c.4829A>T XP_011517718.1:p.Tyr1610Phe
XM_011519417.1:c.4829A>T XP_011517719.1:p.Tyr1610Phe
XM_011519418.1:c.4829A>T XP_011517720.1:p.Tyr1610Phe
XM_011519419.1:c.4730A>T XP_011517721.1:p.Tyr1577Phe
XM_011519420.1:c.4829A>T XP_011517722.1:p.Tyr1610Phe
XM_011519421.1:c.3986A>T XP_011517723.1:p.Tyr1329Phe
XM_011519422.1:c.4829A>T XP_011517724.1:p.Tyr1610Phe
XM_011519423.1:c.3986A>T XP_011517725.1:p.Tyr1329Phe
XM_011519424.1:c.3443A>T XP_011517726.1:p.Tyr1148Phe
XR_930483.1:n.5001A>T
XR_930484.1:n.5001A>T
XM_006717425.4:c.4829A>T XP_006717488.1:p.Tyr1610Phe
XM_011519416.2:c.4829A>T XP_011517718.1:p.Tyr1610Phe
XM_017015928.1:c.4829A>T XP_016871417.1:p.Tyr1610Phe
XM_017015929.1:c.4817A>T XP_016871418.1:p.Tyr1606Phe
XM_017015930.1:c.4829A>T XP_016871419.1:p.Tyr1610Phe
XM_017015931.1:c.4829A>T XP_016871420.1:p.Tyr1610Phe
XM_017015932.1:c.4829A>T XP_016871421.1:p.Tyr1610Phe
XM_017015933.1:c.4829A>T XP_016871422.1:p.Tyr1610Phe
NM_001256053.2:c.3740A>T NP_001242982.1:p.Tyr1247Phe
NM_014915.3:c.3743A>T MANE Select NP_055730.2:p.Tyr1248Phe