Canonical Allele Identifier: CA376357119

Gene: ANKRD26

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27060372T>C , CM000672.2:g.27060372T>C	GRCh38
NC_000010.10:g.27349301T>C , CM000672.1:g.27349301T>C	GRCh37
NC_000010.9:g.27389307T>C	NCBI36
NG_031973.2:g.45127A>G , LRG_605:g.45127A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014915.3:c.1537A>G MANE Select	NP_055730.2:p.Met513Val
ENST00000376087.5:c.1537A>G MANE Select	ENSP00000365255.4:p.Met513Val
NM_001256053.1:c.1537A>G	NP_001242982.1:p.Met513Val
NM_001256053.2:c.1537A>G	NP_001242982.1:p.Met513Val
NM_014915.2:c.1537A>G , LRG_605t1:c.1537A>G	NP_055730.2:p.Met513Val
ENST00000376087.4:c.1537A>G	ENSP00000365255.4:p.Met513Val
ENST00000436985.6:c.1585A>G	ENSP00000405112.2:p.Met529Val
ENST00000436985.7:c.1537A>G	ENSP00000405112.3:p.Met513Val
ENST00000675187.1:c.*876A>G	ENSP00000502611.1:n.*876A>G
ENST00000675846.1:c.1443A>G
ENST00000676232.1:c.1245A>G
ENST00000676420.1:c.*1357A>G	ENSP00000502355.1:n.*1357A>G
XM_006717423.2:c.1537A>G	XP_006717486.1:p.Met513Val
XM_006717424.2:c.1537A>G	XP_006717487.1:p.Met513Val
XM_006717425.2:c.1537A>G	XP_006717488.1:p.Met513Val
XM_006717425.4:c.1537A>G	XP_006717488.1:p.Met513Val
XM_006717427.2:c.694A>G	XP_006717490.1:p.Met232Val
XM_006717428.2:c.1438A>G	XP_006717491.1:p.Met480Val
XM_011519415.1:c.1525A>G	XP_011517717.1:p.Met509Val
XM_011519416.1:c.1537A>G	XP_011517718.1:p.Met513Val
XM_011519416.2:c.1537A>G	XP_011517718.1:p.Met513Val
XM_011519417.1:c.1537A>G	XP_011517719.1:p.Met513Val
XM_011519418.1:c.1537A>G	XP_011517720.1:p.Met513Val
XM_011519419.1:c.1438A>G	XP_011517721.1:p.Met480Val
XM_011519420.1:c.1537A>G	XP_011517722.1:p.Met513Val
XM_011519421.1:c.694A>G	XP_011517723.1:p.Met232Val
XM_011519422.1:c.1537A>G	XP_011517724.1:p.Met513Val
XM_011519423.1:c.694A>G	XP_011517725.1:p.Met232Val
XM_011519424.1:c.151A>G	XP_011517726.1:p.Met51Val
XM_011519425.1:c.1537A>G	XP_011517727.1:p.Met513Val
XM_017015928.1:c.1537A>G	XP_016871417.1:p.Met513Val
XM_017015929.1:c.1525A>G	XP_016871418.1:p.Met509Val
XM_017015930.1:c.1537A>G	XP_016871419.1:p.Met513Val
XM_017015931.1:c.1537A>G	XP_016871420.1:p.Met513Val
XM_017015932.1:c.1537A>G	XP_016871421.1:p.Met513Val
XM_017015933.1:c.1537A>G	XP_016871422.1:p.Met513Val
XM_024447896.1:c.1537A>G	XP_024303664.1:p.Met513Val
XR_930483.1:n.1709A>G
XR_930484.1:n.1709A>G