Canonical Allele Identifier: CA2580613926

Gene: ANKRD11

Linked Data

• ClinVar Variation Id: 2504496
• ClinVar RCV Id: RCV003231957

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89279392_89279393delinsTT , CM000678.2:g.89279392_89279393delinsTT	GRCh38
NC_000016.9:g.89345800_89345801delinsTT , CM000678.1:g.89345800_89345801delinsTT	GRCh37
NC_000016.8:g.87873301_87873302delinsTT	NCBI36
NG_032003.1:g.216169_216170delinsAA
NG_032003.2:g.216169_216170delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301030.10:c.7149_7150delinsAA MANE Select	ENSP00000301030.4:p.His2383_Pro2384delinsGlnThr
ENST00000330736.10:c.*6952_*6953delinsAA	ENSP00000330815.5:n.*6952_*6953delinsAA
ENST00000378330.7:c.7149_7150delinsAA	ENSP00000367581.2:p.His2383_Pro2384delinsGlnThr
ENST00000642600.1:c.7149_7150delinsAA	ENSP00000495226.1:p.His2383_Pro2384delinsGlnThr
ENST00000644285.1:c.745-4202_745-4201delinsAA	ENSP00000496476.1:n.745-4202_745-4201delinsAA
ENST00000301030.8:c.7149_7150delinsAA	ENSP00000301030.4:p.His2383_Pro2384delinsGlnThr
ENST00000330736.9:c.*6952_*6953delinsAA	ENSP00000330815.5:n.*6952_*6953delinsAA
ENST00000378330.6:c.7149_7150delinsAA	ENSP00000367581.2:p.His2383_Pro2384delinsGlnThr
ENST00000562194.1:c.152-4202_152-4201delinsAA
ENST00000623388.1:n.324_325delinsAA
NM_001256182.1:c.7149_7150delinsAA	NP_001243111.1:p.His2383_Pro2384delinsGlnThr
NM_001256183.1:c.7149_7150delinsAA	NP_001243112.1:p.His2383_Pro2384delinsGlnThr
NM_013275.5:c.7149_7150delinsAA	NP_037407.4:p.His2383_Pro2384delinsGlnThr
XM_006721181.1:c.7047_7048delinsAA	XP_006721244.1:p.His2349_Pro2350delinsGlnThr
XM_006721184.2:c.6852_6853delinsAA	XP_006721247.1:p.His2284_Pro2285delinsGlnThr
XM_011523051.1:c.7149_7150delinsAA	XP_011521353.1:p.His2383_Pro2384delinsGlnThr
XM_011523052.1:c.7149_7150delinsAA	XP_011521354.1:p.His2383_Pro2384delinsGlnThr
XM_011523053.1:c.7149_7150delinsAA	XP_011521355.1:p.His2383_Pro2384delinsGlnThr
XM_011523054.1:c.7047_7048delinsAA	XP_011521356.1:p.His2349_Pro2350delinsGlnThr
XM_011523055.1:c.7047_7048delinsAA	XP_011521357.1:p.His2349_Pro2350delinsGlnThr
XM_011523056.1:c.7020_7021delinsAA	XP_011521358.1:p.His2340_Pro2341delinsGlnThr
XM_011523057.1:c.7149_7150delinsAA	XP_011521359.1:p.His2383_Pro2384delinsGlnThr
XM_011523051.3:c.7149_7150delinsAA	XP_011521353.1:p.His2383_Pro2384delinsGlnThr
XM_011523053.2:c.7149_7150delinsAA	XP_011521355.1:p.His2383_Pro2384delinsGlnThr
XM_011523054.2:c.7047_7048delinsAA	XP_011521356.1:p.His2349_Pro2350delinsGlnThr
XM_011523055.2:c.7047_7048delinsAA	XP_011521357.1:p.His2349_Pro2350delinsGlnThr
XM_011523056.2:c.7020_7021delinsAA	XP_011521358.1:p.His2340_Pro2341delinsGlnThr
XM_011523057.2:c.7149_7150delinsAA	XP_011521359.1:p.His2383_Pro2384delinsGlnThr
XM_017023182.2:c.7149_7150delinsAA	XP_016878671.1:p.His2383_Pro2384delinsGlnThr
XM_017023183.1:c.7149_7150delinsAA	XP_016878672.1:p.His2383_Pro2384delinsGlnThr
XM_017023184.1:c.7149_7150delinsAA	XP_016878673.1:p.His2383_Pro2384delinsGlnThr
XM_017023185.1:c.7149_7150delinsAA	XP_016878674.1:p.His2383_Pro2384delinsGlnThr
XM_017023186.1:c.7149_7150delinsAA	XP_016878675.1:p.His2383_Pro2384delinsGlnThr
XM_017023187.1:c.7149_7150delinsAA	XP_016878676.1:p.His2383_Pro2384delinsGlnThr
XM_024450244.1:c.7047_7048delinsAA	XP_024306012.1:p.His2349_Pro2350delinsGlnThr
NM_013275.6:c.7149_7150delinsAA MANE Select	NP_037407.4:p.His2383_Pro2384delinsGlnThr
NM_001256182.2:c.7149_7150delinsAA	NP_001243111.1:p.His2383_Pro2384delinsGlnThr
NM_001256183.2:c.7149_7150delinsAA	NP_001243112.1:p.His2383_Pro2384delinsGlnThr