Canonical Allele Identifier: CA468488072

Gene: ANKRD26

Linked Data

• MyVariant Identifiers: chr10:g.27322214A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27033285A>G , CM000672.2:g.27033285A>G	GRCh38
NC_000010.10:g.27322214A>G , CM000672.1:g.27322214A>G	GRCh37
NC_000010.9:g.27362220A>G	NCBI36
NG_031973.2:g.72214T>C , LRG_605:g.72214T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376087.5:c.3747T>C MANE Select	ENSP00000365255.4:p.Arg1249=
ENST00000436985.7:c.3744T>C	ENSP00000405112.3:p.Arg1248=
ENST00000675116.1:c.1397T>C
ENST00000675936.1:c.163T>C
ENST00000376087.4:c.3747T>C	ENSP00000365255.4:p.Arg1249=
ENST00000436985.6:c.3795T>C	ENSP00000405112.2:p.Arg1265=
NM_001256053.1:c.3744T>C	NP_001242982.1:p.Arg1248=
NM_014915.2:c.3747T>C , LRG_605t1:c.3747T>C	NP_055730.2:p.Arg1249=
XM_006717423.2:c.4833T>C	XP_006717486.1:p.Arg1611=
XM_006717424.2:c.4830T>C	XP_006717487.1:p.Arg1610=
XM_006717425.2:c.4833T>C	XP_006717488.1:p.Arg1611=
XM_006717427.2:c.3990T>C	XP_006717490.1:p.Arg1330=
XM_006717428.2:c.3648T>C	XP_006717491.1:p.Arg1216=
XM_011519415.1:c.4821T>C	XP_011517717.1:p.Arg1607=
XM_011519416.1:c.4833T>C	XP_011517718.1:p.Arg1611=
XM_011519417.1:c.4833T>C	XP_011517719.1:p.Arg1611=
XM_011519418.1:c.4833T>C	XP_011517720.1:p.Arg1611=
XM_011519419.1:c.4734T>C	XP_011517721.1:p.Arg1578=
XM_011519420.1:c.4833T>C	XP_011517722.1:p.Arg1611=
XM_011519421.1:c.3990T>C	XP_011517723.1:p.Arg1330=
XM_011519422.1:c.4833T>C	XP_011517724.1:p.Arg1611=
XM_011519423.1:c.3990T>C	XP_011517725.1:p.Arg1330=
XM_011519424.1:c.3447T>C	XP_011517726.1:p.Arg1149=
XR_930483.1:n.5005T>C
XR_930484.1:n.5005T>C
XM_006717425.4:c.4833T>C	XP_006717488.1:p.Arg1611=
XM_011519416.2:c.4833T>C	XP_011517718.1:p.Arg1611=
XM_017015928.1:c.4833T>C	XP_016871417.1:p.Arg1611=
XM_017015929.1:c.4821T>C	XP_016871418.1:p.Arg1607=
XM_017015930.1:c.4833T>C	XP_016871419.1:p.Arg1611=
XM_017015931.1:c.4833T>C	XP_016871420.1:p.Arg1611=
XM_017015932.1:c.4833T>C	XP_016871421.1:p.Arg1611=
XM_017015933.1:c.4833T>C	XP_016871422.1:p.Arg1611=
NM_001256053.2:c.3744T>C	NP_001242982.1:p.Arg1248=
NM_014915.3:c.3747T>C MANE Select	NP_055730.2:p.Arg1249=