Canonical Allele Identifier: CA5449059

Gene: ANKRD26

Linked Data

• ClinVar Variation Id: 450395
• ClinVar RCV Id: RCV000523525 ; RCV001821459 ; RCV003392351
• dbSNP Id: rs374871257
• ExAC: 10:27389144 G / A
• gnomAD v2: 10-27389144-G-A
• gnomAD v3: 10-27100215-G-A
• gnomAD v4: 10-27100215-G-A
• MyVariant Identifiers: chr10:g.27389144G>A (hg19) ; chr10:g.27100215G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27100215G>A , CM000672.2:g.27100215G>A	GRCh38
NC_000010.10:g.27389144G>A , CM000672.1:g.27389144G>A	GRCh37
NC_000010.9:g.27429150G>A	NCBI36
NG_031973.2:g.5284C>T , LRG_605:g.5284C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376087.5:c.112C>T MANE Select	ENSP00000365255.4:p.Pro38Ser
ENST00000436985.7:c.112C>T	ENSP00000405112.3:p.Pro38Ser
ENST00000675187.1:c.112C>T	ENSP00000502611.1:p.Pro38Ser
ENST00000675846.1:c.84C>T
ENST00000676299.1:c.112C>T	ENSP00000502506.1:p.Pro38Ser
ENST00000676420.1:c.112C>T	ENSP00000502355.1:p.Pro38Ser
ENST00000376087.4:c.112C>T	ENSP00000365255.4:p.Pro38Ser
ENST00000436985.6:c.112C>T	ENSP00000405112.2:p.Pro38Ser
NM_001256053.1:c.112C>T	NP_001242982.1:p.Pro38Ser
NM_014915.2:c.112C>T , LRG_605t1:c.112C>T	NP_055730.2:p.Pro38Ser
XM_006717423.2:c.112C>T	XP_006717486.1:p.Pro38Ser
XM_006717424.2:c.112C>T	XP_006717487.1:p.Pro38Ser
XM_006717425.2:c.112C>T	XP_006717488.1:p.Pro38Ser
XM_006717428.2:c.112C>T	XP_006717491.1:p.Pro38Ser
XM_011519415.1:c.112C>T	XP_011517717.1:p.Pro38Ser
XM_011519416.1:c.112C>T	XP_011517718.1:p.Pro38Ser
XM_011519417.1:c.112C>T	XP_011517719.1:p.Pro38Ser
XM_011519418.1:c.112C>T	XP_011517720.1:p.Pro38Ser
XM_011519419.1:c.112C>T	XP_011517721.1:p.Pro38Ser
XM_011519420.1:c.112C>T	XP_011517722.1:p.Pro38Ser
XM_011519422.1:c.112C>T	XP_011517724.1:p.Pro38Ser
XM_011519425.1:c.112C>T	XP_011517727.1:p.Pro38Ser
XR_930483.1:n.284C>T
XR_930484.1:n.284C>T
XM_006717425.4:c.112C>T	XP_006717488.1:p.Pro38Ser
XM_011519416.2:c.112C>T	XP_011517718.1:p.Pro38Ser
XM_017015928.1:c.112C>T	XP_016871417.1:p.Pro38Ser
XM_017015929.1:c.112C>T	XP_016871418.1:p.Pro38Ser
XM_017015930.1:c.112C>T	XP_016871419.1:p.Pro38Ser
XM_017015931.1:c.112C>T	XP_016871420.1:p.Pro38Ser
XM_017015932.1:c.112C>T	XP_016871421.1:p.Pro38Ser
XM_017015933.1:c.112C>T	XP_016871422.1:p.Pro38Ser
XM_024447896.1:c.112C>T	XP_024303664.1:p.Pro38Ser
NM_001256053.2:c.112C>T	NP_001242982.1:p.Pro38Ser
NM_014915.3:c.112C>T MANE Select	NP_055730.2:p.Pro38Ser