Canonical Allele Identifier: CA376361006

Gene: ANKRD26

Linked Data

• gnomAD v4: 10-27033277-A-C
• MyVariant Identifiers: chr10:g.27322206A>C (hg19) ; chr10:g.27033277A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27033277A>C , CM000672.2:g.27033277A>C	GRCh38
NC_000010.10:g.27322206A>C , CM000672.1:g.27322206A>C	GRCh37
NC_000010.9:g.27362212A>C	NCBI36
NG_031973.2:g.72222T>G , LRG_605:g.72222T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376087.5:c.3755T>G MANE Select	ENSP00000365255.4:p.Leu1252Ter
ENST00000436985.7:c.3752T>G	ENSP00000405112.3:p.Leu1251Ter
ENST00000675116.1:c.1405T>G
ENST00000675936.1:c.171T>G
ENST00000376087.4:c.3755T>G	ENSP00000365255.4:p.Leu1252Ter
ENST00000436985.6:c.3803T>G	ENSP00000405112.2:p.Leu1268Ter
NM_001256053.1:c.3752T>G	NP_001242982.1:p.Leu1251Ter
NM_014915.2:c.3755T>G , LRG_605t1:c.3755T>G	NP_055730.2:p.Leu1252Ter
XM_006717423.2:c.4841T>G	XP_006717486.1:p.Leu1614Ter
XM_006717424.2:c.4838T>G	XP_006717487.1:p.Leu1613Ter
XM_006717425.2:c.4841T>G	XP_006717488.1:p.Leu1614Ter
XM_006717427.2:c.3998T>G	XP_006717490.1:p.Leu1333Ter
XM_006717428.2:c.3656T>G	XP_006717491.1:p.Leu1219Ter
XM_011519415.1:c.4829T>G	XP_011517717.1:p.Leu1610Ter
XM_011519416.1:c.4841T>G	XP_011517718.1:p.Leu1614Ter
XM_011519417.1:c.4841T>G	XP_011517719.1:p.Leu1614Ter
XM_011519418.1:c.4841T>G	XP_011517720.1:p.Leu1614Ter
XM_011519419.1:c.4742T>G	XP_011517721.1:p.Leu1581Ter
XM_011519420.1:c.4841T>G	XP_011517722.1:p.Leu1614Ter
XM_011519421.1:c.3998T>G	XP_011517723.1:p.Leu1333Ter
XM_011519422.1:c.4841T>G	XP_011517724.1:p.Leu1614Ter
XM_011519423.1:c.3998T>G	XP_011517725.1:p.Leu1333Ter
XM_011519424.1:c.3455T>G	XP_011517726.1:p.Leu1152Ter
XR_930483.1:n.5013T>G
XR_930484.1:n.5013T>G
XM_006717425.4:c.4841T>G	XP_006717488.1:p.Leu1614Ter
XM_011519416.2:c.4841T>G	XP_011517718.1:p.Leu1614Ter
XM_017015928.1:c.4841T>G	XP_016871417.1:p.Leu1614Ter
XM_017015929.1:c.4829T>G	XP_016871418.1:p.Leu1610Ter
XM_017015930.1:c.4841T>G	XP_016871419.1:p.Leu1614Ter
XM_017015931.1:c.4841T>G	XP_016871420.1:p.Leu1614Ter
XM_017015932.1:c.4841T>G	XP_016871421.1:p.Leu1614Ter
XM_017015933.1:c.4841T>G	XP_016871422.1:p.Leu1614Ter
NM_001256053.2:c.3752T>G	NP_001242982.1:p.Leu1251Ter
NM_014915.3:c.3755T>G MANE Select	NP_055730.2:p.Leu1252Ter