Canonical Allele Identifier: CA376361326

Gene: ANKRD26

Linked Data

• MyVariant Identifiers: chr10:g.27322307C>A (hg19) ; chr10:g.27033378C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27033378C>A , CM000672.2:g.27033378C>A	GRCh38
NC_000010.10:g.27322307C>A , CM000672.1:g.27322307C>A	GRCh37
NC_000010.9:g.27362313C>A	NCBI36
NG_031973.2:g.72121G>T , LRG_605:g.72121G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376087.5:c.3655-1G>T MANE Select	ENSP00000365255.4:n.3655-1G>T
ENST00000436985.7:c.3652-1G>T	ENSP00000405112.3:n.3652-1G>T
ENST00000675116.1:c.1305-1G>T
ENST00000675936.1:c.71-1G>T
ENST00000376087.4:c.3655-1G>T	ENSP00000365255.4:n.3655-1G>T
ENST00000436985.6:c.3703-1G>T	ENSP00000405112.2:n.3703-1G>T
NM_001256053.1:c.3652-1G>T	NP_001242982.1:n.3652-1G>T
NM_014915.2:c.3655-1G>T , LRG_605t1:c.3655-1G>T	NP_055730.2:n.3655-1G>T
XM_006717423.2:c.4741-1G>T	XP_006717486.1:n.4741-1G>T
XM_006717424.2:c.4738-1G>T	XP_006717487.1:n.4738-1G>T
XM_006717425.2:c.4741-1G>T	XP_006717488.1:n.4741-1G>T
XM_006717427.2:c.3898-1G>T	XP_006717490.1:n.3898-1G>T
XM_006717428.2:c.3556-1G>T	XP_006717491.1:n.3556-1G>T
XM_011519415.1:c.4729-1G>T	XP_011517717.1:n.4729-1G>T
XM_011519416.1:c.4741-1G>T	XP_011517718.1:n.4741-1G>T
XM_011519417.1:c.4741-1G>T	XP_011517719.1:n.4741-1G>T
XM_011519418.1:c.4741-1G>T	XP_011517720.1:n.4741-1G>T
XM_011519419.1:c.4642-1G>T	XP_011517721.1:n.4642-1G>T
XM_011519420.1:c.4741-1G>T	XP_011517722.1:n.4741-1G>T
XM_011519421.1:c.3898-1G>T	XP_011517723.1:n.3898-1G>T
XM_011519422.1:c.4741-1G>T	XP_011517724.1:n.4741-1G>T
XM_011519423.1:c.3898-1G>T	XP_011517725.1:n.3898-1G>T
XM_011519424.1:c.3355-1G>T	XP_011517726.1:n.3355-1G>T
XM_011519425.1:c.*16G>T	XP_011517727.1:n.*16G>T
XR_930483.1:n.4913-1G>T
XR_930484.1:n.4913-1G>T
XM_006717425.4:c.4741-1G>T	XP_006717488.1:n.4741-1G>T
XM_011519416.2:c.4741-1G>T	XP_011517718.1:n.4741-1G>T
XM_017015928.1:c.4741-1G>T	XP_016871417.1:n.4741-1G>T
XM_017015929.1:c.4729-1G>T	XP_016871418.1:n.4729-1G>T
XM_017015930.1:c.4741-1G>T	XP_016871419.1:n.4741-1G>T
XM_017015931.1:c.4741-1G>T	XP_016871420.1:n.4741-1G>T
XM_017015932.1:c.4741-1G>T	XP_016871421.1:n.4741-1G>T
XM_017015933.1:c.4741-1G>T	XP_016871422.1:n.4741-1G>T
NM_001256053.2:c.3652-1G>T	NP_001242982.1:n.3652-1G>T
NM_014915.3:c.3655-1G>T MANE Select	NP_055730.2:n.3655-1G>T