Canonical Allele Identifier: CA624452407

Gene: ANKRD11

Linked Data

• dbSNP Id: rs1470287881
• gnomAD v2: 16-89350851-AGTTTCTCTTCTTTTT-A
• gnomAD v4: 16-89284443-AGTTTCTCTTCTTTTT-A
• MyVariant Identifiers: chr16:g.89350852_89350866del (hg19) ; chr16:g.89284444_89284458del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89284444_89284458del , CM000678.2:g.89284444_89284458del	GRCh38
NC_000016.9:g.89350852_89350866del , CM000678.1:g.89350852_89350866del	GRCh37
NC_000016.8:g.87878353_87878367del	NCBI36
NG_032003.1:g.211104_211118del
NG_032003.2:g.211104_211118del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301030.10:c.2084_2098del MANE Select	ENSP00000301030.4:p.Lys695_Leu700delinsIle
ENST00000330736.10:c.*1887_*1901del	ENSP00000330815.5:n.*1887_*1901del
ENST00000378330.7:c.2084_2098del	ENSP00000367581.2:p.Lys695_Leu700delinsIle
ENST00000642443.1:c.1709_1723del	ENSP00000493644.1:p.Lys570_Leu575delinsIle
ENST00000642600.1:c.2084_2098del	ENSP00000495226.1:p.Lys695_Leu700delinsIle
ENST00000644285.1:c.744+4070_744+4084del	ENSP00000496476.1:n.744+4070_744+4084del
ENST00000645212.1:n.3856_3870del
ENST00000301030.8:c.2084_2098del	ENSP00000301030.4:p.Lys695_Leu700delinsIle
ENST00000330736.9:c.*1887_*1901del	ENSP00000330815.5:n.*1887_*1901del
ENST00000378330.6:c.2084_2098del	ENSP00000367581.2:p.Lys695_Leu700delinsIle
ENST00000562194.1:c.151+4070_151+4084del
NM_001256182.1:c.2084_2098del	NP_001243111.1:p.Lys695_Leu700delinsIle
NM_001256183.1:c.2084_2098del	NP_001243112.1:p.Lys695_Leu700delinsIle
NM_013275.5:c.2084_2098del	NP_037407.4:p.Lys695_Leu700delinsIle
XM_006721181.1:c.1982_1996del	XP_006721244.1:p.Lys661_Leu666delinsIle
XM_006721184.2:c.1787_1801del	XP_006721247.1:p.Lys596_Leu601delinsIle
XM_011523051.1:c.2084_2098del	XP_011521353.1:p.Lys695_Leu700delinsIle
XM_011523052.1:c.2084_2098del	XP_011521354.1:p.Lys695_Leu700delinsIle
XM_011523053.1:c.2084_2098del	XP_011521355.1:p.Lys695_Leu700delinsIle
XM_011523054.1:c.1982_1996del	XP_011521356.1:p.Lys661_Leu666delinsIle
XM_011523055.1:c.1982_1996del	XP_011521357.1:p.Lys661_Leu666delinsIle
XM_011523056.1:c.1955_1969del	XP_011521358.1:p.Lys652_Leu657delinsIle
XM_011523057.1:c.2084_2098del	XP_011521359.1:p.Lys695_Leu700delinsIle
XM_011523051.3:c.2084_2098del	XP_011521353.1:p.Lys695_Leu700delinsIle
XM_011523053.2:c.2084_2098del	XP_011521355.1:p.Lys695_Leu700delinsIle
XM_011523054.2:c.1982_1996del	XP_011521356.1:p.Lys661_Leu666delinsIle
XM_011523055.2:c.1982_1996del	XP_011521357.1:p.Lys661_Leu666delinsIle
XM_011523056.2:c.1955_1969del	XP_011521358.1:p.Lys652_Leu657delinsIle
XM_011523057.2:c.2084_2098del	XP_011521359.1:p.Lys695_Leu700delinsIle
XM_017023182.2:c.2084_2098del	XP_016878671.1:p.Lys695_Leu700delinsIle
XM_017023183.1:c.2084_2098del	XP_016878672.1:p.Lys695_Leu700delinsIle
XM_017023184.1:c.2084_2098del	XP_016878673.1:p.Lys695_Leu700delinsIle
XM_017023185.1:c.2084_2098del	XP_016878674.1:p.Lys695_Leu700delinsIle
XM_017023186.1:c.2084_2098del	XP_016878675.1:p.Lys695_Leu700delinsIle
XM_017023187.1:c.2084_2098del	XP_016878676.1:p.Lys695_Leu700delinsIle
XM_024450244.1:c.1982_1996del	XP_024306012.1:p.Lys661_Leu666delinsIle
NM_013275.6:c.2084_2098del MANE Select	NP_037407.4:p.Lys695_Leu700delinsIle
NM_001256182.2:c.2084_2098del	NP_001243111.1:p.Lys695_Leu700delinsIle
NM_001256183.2:c.2084_2098del	NP_001243112.1:p.Lys695_Leu700delinsIle