Canonical Allele Identifier: CA397163853

Gene: ANKRD11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89305206C>T , CM000678.2:g.89305206C>T	GRCh38
NC_000016.9:g.89371614C>T , CM000678.1:g.89371614C>T	GRCh37
NC_000016.8:g.87899115C>T	NCBI36
NG_032003.1:g.190356G>A
NG_032003.2:g.190356G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_013275.6:c.226G>A MANE Select	NP_037407.4:p.Glu76Lys
ENST00000301030.10:c.226G>A MANE Select	ENSP00000301030.4:p.Glu76Lys
NM_001256182.1:c.226G>A	NP_001243111.1:p.Glu76Lys
NM_001256182.2:c.226G>A	NP_001243111.1:p.Glu76Lys
NM_001256183.1:c.226G>A	NP_001243112.1:p.Glu76Lys
NM_001256183.2:c.226G>A	NP_001243112.1:p.Glu76Lys
NM_013275.5:c.226G>A	NP_037407.4:p.Glu76Lys
NR_045839.1:n.960G>A
NR_045839.2:n.960G>A
ENST00000301030.8:c.226G>A	ENSP00000301030.4:p.Glu76Lys
ENST00000330736.10:c.226G>A	ENSP00000330815.5:p.Asp76Asn
ENST00000330736.9:c.226G>A	ENSP00000330815.5:p.Asp76Asn
ENST00000378330.6:c.226G>A	ENSP00000367581.2:p.Glu76Lys
ENST00000378330.7:c.226G>A	ENSP00000367581.2:p.Glu76Lys
ENST00000378332.6:c.*391G>A	ENSP00000367583.2:n.*391G>A
ENST00000378332.7:c.*391G>A	ENSP00000367583.2:n.*391G>A
ENST00000562275.5:c.226G>A	ENSP00000454550.1:p.Asp76Asn
ENST00000562275.6:c.226G>A	ENSP00000454550.1:p.Asp76Asn
ENST00000562816.5:n.523G>A
ENST00000563291.1:c.226G>A	ENSP00000455008.1:p.Gly76Arg
ENST00000564553.5:n.259G>A
ENST00000566858.5:n.383G>A
ENST00000567699.1:n.285G>A
ENST00000567699.2:n.443G>A
ENST00000567736.5:n.663G>A
ENST00000567736.6:c.226G>A	ENSP00000496367.1:p.Gly76Arg
ENST00000568924.1:n.270-4244G>A
ENST00000613312.4:c.226G>A	ENSP00000478018.1:p.Glu76Lys
ENST00000642333.1:c.226G>A	ENSP00000496651.1:p.Glu76Lys
ENST00000642443.1:c.226G>A	ENSP00000493644.1:p.Gly76Ser
ENST00000642600.1:c.226G>A	ENSP00000495226.1:p.Glu76Lys
ENST00000642695.1:c.226G>A	ENSP00000495449.1:p.Glu76Lys
ENST00000643147.1:n.412G>A
ENST00000643964.1:c.226G>A	ENSP00000495181.1:p.Asp76Asn
ENST00000644045.1:c.226G>A	ENSP00000496636.1:p.Glu76Lys
ENST00000644285.1:c.226G>A	ENSP00000496476.1:p.Glu76Lys
ENST00000644784.1:c.226G>A	ENSP00000496419.1:p.Glu76Lys
ENST00000645278.1:c.226G>A	ENSP00000494850.1:p.Val76Met
ENST00000645664.1:c.67-4244G>A	ENSP00000495975.1:n.67-4244G>A
ENST00000645844.1:n.398G>A
ENST00000646166.1:c.148G>A	ENSP00000493980.1:p.Glu50Lys
ENST00000646345.1:n.34G>A
ENST00000646838.1:c.226G>A	ENSP00000495124.1:p.Glu76Lys
ENST00000646975.1:c.226G>A	ENSP00000495608.1:p.Glu76Lys
ENST00000647213.1:c.27G>A	ENSP00000495399.1:p.Gln9=
ENST00000647238.1:c.226G>A	ENSP00000496656.1:p.Gly76Arg
XM_006721181.1:c.27G>A	XP_006721244.1:p.Gln9=
XM_006721184.2:c.-72G>A	XP_006721247.1:n.-72G>A
XM_011523051.1:c.226G>A	XP_011521353.1:p.Glu76Lys
XM_011523051.3:c.226G>A	XP_011521353.1:p.Glu76Lys
XM_011523052.1:c.226G>A	XP_011521354.1:p.Glu76Lys
XM_011523053.1:c.226G>A	XP_011521355.1:p.Glu76Lys
XM_011523053.2:c.226G>A	XP_011521355.1:p.Glu76Lys
XM_011523054.1:c.27G>A	XP_011521356.1:p.Gln9=
XM_011523054.2:c.27G>A	XP_011521356.1:p.Gln9=
XM_011523055.1:c.27G>A	XP_011521357.1:p.Gln9=
XM_011523055.2:c.27G>A	XP_011521357.1:p.Gln9=
XM_011523056.1:c.-23G>A	XP_011521358.1:n.-23G>A
XM_011523056.2:c.-23G>A	XP_011521358.1:n.-23G>A
XM_011523057.1:c.226G>A	XP_011521359.1:p.Glu76Lys
XM_011523057.2:c.226G>A	XP_011521359.1:p.Glu76Lys
XM_017023182.2:c.226G>A	XP_016878671.1:p.Glu76Lys
XM_017023183.1:c.226G>A	XP_016878672.1:p.Glu76Lys
XM_017023184.1:c.226G>A	XP_016878673.1:p.Glu76Lys
XM_017023185.1:c.226G>A	XP_016878674.1:p.Glu76Lys
XM_017023186.1:c.226G>A	XP_016878675.1:p.Glu76Lys
XM_017023187.1:c.226G>A	XP_016878676.1:p.Glu76Lys
XM_024450244.1:c.27G>A	XP_024306012.1:p.Gln9=