Canonical Allele Identifier: CA2573152761

Gene: ANKRD11

Linked Data

• ClinVar Variation Id: 1677123
• ClinVar RCV Id: RCV002222981
• dbSNP Id: rs2151660554

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89268532_89268533dup , CM000678.2:g.89268532_89268533dup	GRCh38
NC_000016.9:g.89334940_89334941dup , CM000678.1:g.89334940_89334941dup	GRCh37
NC_000016.8:g.87862441_87862442dup	NCBI36
NG_032003.1:g.227029_227030dup
NG_032003.2:g.227029_227030dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301030.10:c.7937_7938dup MANE Select	ENSP00000301030.4:p.Phe2647ProfsTer?
ENST00000330736.10:c.*7740_*7741dup	ENSP00000330815.5:n.*7740_*7741dup
ENST00000378330.7:c.7937_7938dup	ENSP00000367581.2:p.Phe2647ProfsTer?
ENST00000642600.1:c.7937_7938dup	ENSP00000495226.1:p.Phe2647ProfsTer?
ENST00000644285.1:c.1211_1212dup	ENSP00000496476.1:p.Phe405ProfsTer?
ENST00000301030.8:c.7937_7938dup	ENSP00000301030.4:p.Phe2647ProfsTer?
ENST00000330736.9:c.*7740_*7741dup	ENSP00000330815.5:n.*7740_*7741dup
ENST00000378330.6:c.7937_7938dup	ENSP00000367581.2:p.Phe2647ProfsTer?
NM_001256182.1:c.7937_7938dup	NP_001243111.1:p.Phe2647ProfsTer?
NM_001256183.1:c.7937_7938dup	NP_001243112.1:p.Phe2647ProfsTer?
NM_013275.5:c.7937_7938dup	NP_037407.4:p.Phe2647ProfsTer?
XM_006721181.1:c.7835_7836dup	XP_006721244.1:p.Phe2613ProfsTer?
XM_006721184.2:c.7640_7641dup	XP_006721247.1:p.Phe2548ProfsTer?
XM_011523051.1:c.7937_7938dup	XP_011521353.1:p.Phe2647ProfsTer?
XM_011523052.1:c.7937_7938dup	XP_011521354.1:p.Phe2647ProfsTer?
XM_011523053.1:c.7937_7938dup	XP_011521355.1:p.Phe2647ProfsTer?
XM_011523054.1:c.7835_7836dup	XP_011521356.1:p.Phe2613ProfsTer?
XM_011523055.1:c.7835_7836dup	XP_011521357.1:p.Phe2613ProfsTer?
XM_011523056.1:c.7808_7809dup	XP_011521358.1:p.Phe2604ProfsTer?
XM_011523051.3:c.7937_7938dup	XP_011521353.1:p.Phe2647ProfsTer?
XM_011523053.2:c.7937_7938dup	XP_011521355.1:p.Phe2647ProfsTer?
XM_011523054.2:c.7835_7836dup	XP_011521356.1:p.Phe2613ProfsTer?
XM_011523055.2:c.7835_7836dup	XP_011521357.1:p.Phe2613ProfsTer?
XM_011523056.2:c.7808_7809dup	XP_011521358.1:p.Phe2604ProfsTer?
XM_017023182.2:c.7937_7938dup	XP_016878671.1:p.Phe2647ProfsTer?
XM_017023183.1:c.7937_7938dup	XP_016878672.1:p.Phe2647ProfsTer?
XM_017023184.1:c.7937_7938dup	XP_016878673.1:p.Phe2647ProfsTer?
XM_017023185.1:c.7937_7938dup	XP_016878674.1:p.Phe2647ProfsTer?
XM_017023186.1:c.7937_7938dup	XP_016878675.1:p.Phe2647ProfsTer?
XM_017023187.1:c.7937_7938dup	XP_016878676.1:p.Phe2647ProfsTer?
XM_024450244.1:c.7835_7836dup	XP_024306012.1:p.Phe2613ProfsTer?
NM_013275.6:c.7937_7938dup MANE Select	NP_037407.4:p.Phe2647ProfsTer?
NM_001256182.2:c.7937_7938dup	NP_001243111.1:p.Phe2647ProfsTer?
NM_001256183.2:c.7937_7938dup	NP_001243112.1:p.Phe2647ProfsTer?