Canonical Allele Identifier: CA5447822
Community Standard Title: NM_014915.3(ANKRD26):c.4249G>C (p.Gly1417Arg)
Gene: ANKRD26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27017759C>G , CM000672.2:g.27017759C>G GRCh38
NC_000010.10:g.27306688C>G , CM000672.1:g.27306688C>G GRCh37
NC_000010.9:g.27346694C>G NCBI36
NG_031973.2:g.87740G>C , LRG_605:g.87740G>C

Transcript Alleles

HGVS Amino-acid Change
NM_014915.3:c.4249G>C MANE Select NP_055730.2:p.Gly1417Arg
ENST00000376087.5:c.4249G>C MANE Select ENSP00000365255.4:p.Gly1417Arg
NM_001256053.1:c.4246G>C NP_001242982.1:p.Gly1416Arg
NM_001256053.2:c.4246G>C NP_001242982.1:p.Gly1416Arg
NM_014915.2:c.4249G>C , LRG_605t1:c.4249G>C NP_055730.2:p.Gly1417Arg
ENST00000376087.4:c.4249G>C ENSP00000365255.4:p.Gly1417Arg
ENST00000436985.6:c.4297G>C ENSP00000405112.2:p.Gly1433Arg
ENST00000436985.7:c.4246G>C ENSP00000405112.3:p.Gly1416Arg
ENST00000675116.1:c.2107G>C
ENST00000675936.1:c.665G>C
ENST00000676280.1:c.78G>C
XM_006717423.2:c.5335G>C XP_006717486.1:p.Gly1779Arg
XM_006717424.2:c.5332G>C XP_006717487.1:p.Gly1778Arg
XM_006717425.2:c.5335G>C XP_006717488.1:p.Gly1779Arg
XM_006717425.4:c.5335G>C XP_006717488.1:p.Gly1779Arg
XM_006717427.2:c.4492G>C XP_006717490.1:p.Gly1498Arg
XM_006717428.2:c.4150G>C XP_006717491.1:p.Gly1384Arg
XM_011519415.1:c.5323G>C XP_011517717.1:p.Gly1775Arg
XM_011519416.1:c.5335G>C XP_011517718.1:p.Gly1779Arg
XM_011519416.2:c.5335G>C XP_011517718.1:p.Gly1779Arg
XM_011519417.1:c.5335G>C XP_011517719.1:p.Gly1779Arg
XM_011519418.1:c.5335G>C XP_011517720.1:p.Gly1779Arg
XM_011519419.1:c.5236G>C XP_011517721.1:p.Gly1746Arg
XM_011519420.1:c.5302-3048G>C XP_011517722.1:n.5302-3048G>C
XM_011519421.1:c.4492G>C XP_011517723.1:p.Gly1498Arg
XM_011519423.1:c.4492G>C XP_011517725.1:p.Gly1498Arg
XM_011519424.1:c.3949G>C XP_011517726.1:p.Gly1317Arg
XM_017015928.1:c.5335G>C XP_016871417.1:p.Gly1779Arg
XM_017015929.1:c.5323G>C XP_016871418.1:p.Gly1775Arg
XM_017015930.1:c.5335G>C XP_016871419.1:p.Gly1779Arg
XM_017015931.1:c.5335G>C XP_016871420.1:p.Gly1779Arg
XM_017015932.1:c.5335G>C XP_016871421.1:p.Gly1779Arg
XM_017015933.1:c.*572G>C XP_016871422.1:n.*572G>C
XR_930483.1:n.5507G>C
XR_930484.1:n.5507G>C