Canonical Allele Identifier: CA376361020

Gene: ANKRD26

Linked Data

• MyVariant Identifiers: chr10:g.27322212A>C (hg19) ; chr10:g.27033283A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27033283A>C , CM000672.2:g.27033283A>C	GRCh38
NC_000010.10:g.27322212A>C , CM000672.1:g.27322212A>C	GRCh37
NC_000010.9:g.27362218A>C	NCBI36
NG_031973.2:g.72216T>G , LRG_605:g.72216T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376087.5:c.3749T>G MANE Select	ENSP00000365255.4:p.Ile1250Ser
ENST00000436985.7:c.3746T>G	ENSP00000405112.3:p.Ile1249Ser
ENST00000675116.1:c.1399T>G
ENST00000675936.1:c.165T>G
ENST00000376087.4:c.3749T>G	ENSP00000365255.4:p.Ile1250Ser
ENST00000436985.6:c.3797T>G	ENSP00000405112.2:p.Ile1266Ser
NM_001256053.1:c.3746T>G	NP_001242982.1:p.Ile1249Ser
NM_014915.2:c.3749T>G , LRG_605t1:c.3749T>G	NP_055730.2:p.Ile1250Ser
XM_006717423.2:c.4835T>G	XP_006717486.1:p.Ile1612Ser
XM_006717424.2:c.4832T>G	XP_006717487.1:p.Ile1611Ser
XM_006717425.2:c.4835T>G	XP_006717488.1:p.Ile1612Ser
XM_006717427.2:c.3992T>G	XP_006717490.1:p.Ile1331Ser
XM_006717428.2:c.3650T>G	XP_006717491.1:p.Ile1217Ser
XM_011519415.1:c.4823T>G	XP_011517717.1:p.Ile1608Ser
XM_011519416.1:c.4835T>G	XP_011517718.1:p.Ile1612Ser
XM_011519417.1:c.4835T>G	XP_011517719.1:p.Ile1612Ser
XM_011519418.1:c.4835T>G	XP_011517720.1:p.Ile1612Ser
XM_011519419.1:c.4736T>G	XP_011517721.1:p.Ile1579Ser
XM_011519420.1:c.4835T>G	XP_011517722.1:p.Ile1612Ser
XM_011519421.1:c.3992T>G	XP_011517723.1:p.Ile1331Ser
XM_011519422.1:c.4835T>G	XP_011517724.1:p.Ile1612Ser
XM_011519423.1:c.3992T>G	XP_011517725.1:p.Ile1331Ser
XM_011519424.1:c.3449T>G	XP_011517726.1:p.Ile1150Ser
XR_930483.1:n.5007T>G
XR_930484.1:n.5007T>G
XM_006717425.4:c.4835T>G	XP_006717488.1:p.Ile1612Ser
XM_011519416.2:c.4835T>G	XP_011517718.1:p.Ile1612Ser
XM_017015928.1:c.4835T>G	XP_016871417.1:p.Ile1612Ser
XM_017015929.1:c.4823T>G	XP_016871418.1:p.Ile1608Ser
XM_017015930.1:c.4835T>G	XP_016871419.1:p.Ile1612Ser
XM_017015931.1:c.4835T>G	XP_016871420.1:p.Ile1612Ser
XM_017015932.1:c.4835T>G	XP_016871421.1:p.Ile1612Ser
XM_017015933.1:c.4835T>G	XP_016871422.1:p.Ile1612Ser
NM_001256053.2:c.3746T>G	NP_001242982.1:p.Ile1249Ser
NM_014915.3:c.3749T>G MANE Select	NP_055730.2:p.Ile1250Ser