Canonical Allele Identifier: CA207188

Gene: ANKRD26

Linked Data

• ClinVar Variation Id: 210183
• ClinVar RCV Id: RCV000193597
• dbSNP Id: rs797045239
• gnomAD v4: 10-27093874-ACATTAAATAG-A
• MyVariant Identifiers: chr10:g.27382804_27382813del (hg19) ; chr10:g.27093875_27093884del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27093878_27093887del , CM000672.2:g.27093878_27093887del	GRCh38
NC_000010.10:g.27382807_27382816del , CM000672.1:g.27382807_27382816del	GRCh37
NC_000010.9:g.27422813_27422822del	NCBI36
NG_031973.2:g.11615_11624del , LRG_605:g.11615_11624del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376087.5:c.243-85_243-76del MANE Select	ENSP00000365255.4:n.243-85_243-76del
ENST00000436985.7:c.243-85_243-76del	ENSP00000405112.3:n.243-85_243-76del
ENST00000674697.1:c.84-85_84-76del	ENSP00000502724.1:n.84-85_84-76del
ENST00000675187.1:c.243-1372_243-1363del	ENSP00000502611.1:n.243-1372_243-1363del
ENST00000675846.1:c.215-85_215-76del
ENST00000676232.1:c.50-85_50-76del
ENST00000676299.1:c.243-85_243-76del	ENSP00000502506.1:n.243-85_243-76del
ENST00000676361.1:c.87-85_87-76del	ENSP00000502704.1:n.87-85_87-76del
ENST00000676420.1:c.*63-85_*63-76del	ENSP00000502355.1:n.*63-85_*63-76del
ENST00000376087.4:c.243-85_243-76del	ENSP00000365255.4:n.243-85_243-76del
ENST00000436985.6:c.243-85_243-76del	ENSP00000405112.2:n.243-85_243-76del
NM_001256053.1:c.243-85_243-76del	NP_001242982.1:n.243-85_243-76del
NM_014915.2:c.243-85_243-76del , LRG_605t1:c.243-85_243-76del	NP_055730.2:n.243-85_243-76del
XM_006717423.2:c.243-85_243-76del	XP_006717486.1:n.243-85_243-76del
XM_006717424.2:c.243-85_243-76del	XP_006717487.1:n.243-85_243-76del
XM_006717425.2:c.243-85_243-76del	XP_006717488.1:n.243-85_243-76del
XM_006717428.2:c.243-85_243-76del	XP_006717491.1:n.243-85_243-76del
XM_011519415.1:c.243-85_243-76del	XP_011517717.1:n.243-85_243-76del
XM_011519416.1:c.243-85_243-76del	XP_011517718.1:n.243-85_243-76del
XM_011519417.1:c.243-85_243-76del	XP_011517719.1:n.243-85_243-76del
XM_011519418.1:c.243-85_243-76del	XP_011517720.1:n.243-85_243-76del
XM_011519419.1:c.243-85_243-76del	XP_011517721.1:n.243-85_243-76del
XM_011519420.1:c.243-85_243-76del	XP_011517722.1:n.243-85_243-76del
XM_011519422.1:c.243-85_243-76del	XP_011517724.1:n.243-85_243-76del
XM_011519425.1:c.243-85_243-76del	XP_011517727.1:n.243-85_243-76del
XR_930483.1:n.415-85_415-76del
XR_930484.1:n.415-85_415-76del
XM_006717425.4:c.243-85_243-76del	XP_006717488.1:n.243-85_243-76del
XM_011519416.2:c.243-85_243-76del	XP_011517718.1:n.243-85_243-76del
XM_017015928.1:c.243-85_243-76del	XP_016871417.1:n.243-85_243-76del
XM_017015929.1:c.243-85_243-76del	XP_016871418.1:n.243-85_243-76del
XM_017015930.1:c.243-85_243-76del	XP_016871419.1:n.243-85_243-76del
XM_017015931.1:c.243-85_243-76del	XP_016871420.1:n.243-85_243-76del
XM_017015932.1:c.243-85_243-76del	XP_016871421.1:n.243-85_243-76del
XM_017015933.1:c.243-85_243-76del	XP_016871422.1:n.243-85_243-76del
XM_024447896.1:c.243-85_243-76del	XP_024303664.1:n.243-85_243-76del
NM_001256053.2:c.243-85_243-76del	NP_001242982.1:n.243-85_243-76del
NM_014915.3:c.243-85_243-76del MANE Select	NP_055730.2:n.243-85_243-76del