Canonical Allele Identifier: CA2580613925

Gene: ANKRD11

Linked Data

• ClinVar Variation Id: 1303861
• ClinVar RCV Id: RCV001758154
• dbSNP Id: rs2151661123

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89268656_89268658del , CM000678.2:g.89268656_89268658del	GRCh38
NC_000016.9:g.89335064_89335066del , CM000678.1:g.89335064_89335066del	GRCh37
NC_000016.8:g.87862565_87862567del	NCBI36
NG_032003.1:g.226908_226910del
NG_032003.2:g.226908_226910del

Transcript Alleles

HGVS	Amino-acid change
ENST00000301030.10:c.7816_7818del MANE Select	ENSP00000301030.4:p.Leu2606del
ENST00000330736.10:c.*7619_*7621del	ENSP00000330815.5:n.*7619_*7621del
ENST00000378330.7:c.7816_7818del	ENSP00000367581.2:p.Leu2606del
ENST00000642600.1:c.7816_7818del	ENSP00000495226.1:p.Leu2606del
ENST00000644285.1:c.1090_1092del	ENSP00000496476.1:p.Leu364del
ENST00000301030.8:c.7816_7818del	ENSP00000301030.4:p.Leu2606del
ENST00000330736.9:c.*7619_*7621del	ENSP00000330815.5:n.*7619_*7621del
ENST00000378330.6:c.7816_7818del	ENSP00000367581.2:p.Leu2606del
ENST00000562194.1:c.497_499del
NM_001256182.1:c.7816_7818del	NP_001243111.1:p.Leu2606del
NM_001256183.1:c.7816_7818del	NP_001243112.1:p.Leu2606del
NM_013275.5:c.7816_7818del	NP_037407.4:p.Leu2606del
XM_006721181.1:c.7714_7716del	XP_006721244.1:p.Leu2572del
XM_006721184.2:c.7519_7521del	XP_006721247.1:p.Leu2507del
XM_011523051.1:c.7816_7818del	XP_011521353.1:p.Leu2606del
XM_011523052.1:c.7816_7818del	XP_011521354.1:p.Leu2606del
XM_011523053.1:c.7816_7818del	XP_011521355.1:p.Leu2606del
XM_011523054.1:c.7714_7716del	XP_011521356.1:p.Leu2572del
XM_011523055.1:c.7714_7716del	XP_011521357.1:p.Leu2572del
XM_011523056.1:c.7687_7689del	XP_011521358.1:p.Leu2563del
XM_011523051.3:c.7816_7818del	XP_011521353.1:p.Leu2606del
XM_011523053.2:c.7816_7818del	XP_011521355.1:p.Leu2606del
XM_011523054.2:c.7714_7716del	XP_011521356.1:p.Leu2572del
XM_011523055.2:c.7714_7716del	XP_011521357.1:p.Leu2572del
XM_011523056.2:c.7687_7689del	XP_011521358.1:p.Leu2563del
XM_017023182.2:c.7816_7818del	XP_016878671.1:p.Leu2606del
XM_017023183.1:c.7816_7818del	XP_016878672.1:p.Leu2606del
XM_017023184.1:c.7816_7818del	XP_016878673.1:p.Leu2606del
XM_017023185.1:c.7816_7818del	XP_016878674.1:p.Leu2606del
XM_017023186.1:c.7816_7818del	XP_016878675.1:p.Leu2606del
XM_017023187.1:c.7816_7818del	XP_016878676.1:p.Leu2606del
XM_024450244.1:c.7714_7716del	XP_024306012.1:p.Leu2572del
NM_013275.6:c.7816_7818del MANE Select	NP_037407.4:p.Leu2606del
NM_001256182.2:c.7816_7818del	NP_001243111.1:p.Leu2606del
NM_001256183.2:c.7816_7818del	NP_001243112.1:p.Leu2606del