Canonical Allele Identifier: CA397163849

Gene: ANKRD11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89305205C>T , CM000678.2:g.89305205C>T	GRCh38
NC_000016.9:g.89371613C>T , CM000678.1:g.89371613C>T	GRCh37
NC_000016.8:g.87899114C>T	NCBI36
NG_032003.1:g.190357G>A
NG_032003.2:g.190357G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_013275.6:c.226+1G>A MANE Select	NP_037407.4:n.226+1G>A
ENST00000301030.10:c.226+1G>A MANE Select	ENSP00000301030.4:n.226+1G>A
NM_001256182.1:c.226+1G>A	NP_001243111.1:n.226+1G>A
NM_001256182.2:c.226+1G>A	NP_001243111.1:n.226+1G>A
NM_001256183.1:c.226+1G>A	NP_001243112.1:n.226+1G>A
NM_001256183.2:c.226+1G>A	NP_001243112.1:n.226+1G>A
NM_013275.5:c.226+1G>A	NP_037407.4:n.226+1G>A
NR_045839.1:n.960+1G>A
NR_045839.2:n.960+1G>A
ENST00000301030.8:c.226+1G>A	ENSP00000301030.4:n.226+1G>A
ENST00000330736.10:c.226+1G>A	ENSP00000330815.5:n.226+1G>A
ENST00000330736.9:c.226+1G>A	ENSP00000330815.5:n.226+1G>A
ENST00000378330.6:c.226+1G>A	ENSP00000367581.2:n.226+1G>A
ENST00000378330.7:c.226+1G>A	ENSP00000367581.2:n.226+1G>A
ENST00000378332.6:c.*391+1G>A	ENSP00000367583.2:n.*391+1G>A
ENST00000378332.7:c.*391+1G>A	ENSP00000367583.2:n.*391+1G>A
ENST00000562275.5:c.226+1G>A	ENSP00000454550.1:n.226+1G>A
ENST00000562275.6:c.226+1G>A	ENSP00000454550.1:n.226+1G>A
ENST00000562816.5:n.523+1G>A
ENST00000563291.1:c.226+1G>A	ENSP00000455008.1:n.226+1G>A
ENST00000564553.5:n.259+1G>A
ENST00000566858.5:n.383+1G>A
ENST00000567699.1:n.285+1G>A
ENST00000567699.2:n.443+1G>A
ENST00000567736.5:n.663+1G>A
ENST00000567736.6:c.226+1G>A	ENSP00000496367.1:n.226+1G>A
ENST00000568924.1:n.270-4243G>A
ENST00000613312.4:c.226+1G>A	ENSP00000478018.1:n.226+1G>A
ENST00000642333.1:c.226+1G>A	ENSP00000496651.1:n.226+1G>A
ENST00000642443.1:c.226+1G>A	ENSP00000493644.1:n.226+1G>A
ENST00000642600.1:c.226+1G>A	ENSP00000495226.1:n.226+1G>A
ENST00000642695.1:c.226+1G>A	ENSP00000495449.1:n.226+1G>A
ENST00000643147.1:n.413G>A
ENST00000643964.1:c.226+1G>A	ENSP00000495181.1:n.226+1G>A
ENST00000644045.1:c.226+1G>A	ENSP00000496636.1:n.226+1G>A
ENST00000644285.1:c.226+1G>A	ENSP00000496476.1:n.226+1G>A
ENST00000644784.1:c.226+1G>A	ENSP00000496419.1:n.226+1G>A
ENST00000645278.1:c.226+1G>A	ENSP00000494850.1:n.226+1G>A
ENST00000645664.1:c.67-4243G>A	ENSP00000495975.1:n.67-4243G>A
ENST00000645844.1:n.398+1G>A
ENST00000646166.1:c.148+1G>A	ENSP00000493980.1:n.148+1G>A
ENST00000646345.1:n.34+1G>A
ENST00000646838.1:c.226+1G>A	ENSP00000495124.1:n.226+1G>A
ENST00000646975.1:c.226+1G>A	ENSP00000495608.1:n.226+1G>A
ENST00000647213.1:c.27+1G>A	ENSP00000495399.1:n.27+1G>A
ENST00000647238.1:c.226+1G>A	ENSP00000496656.1:n.226+1G>A
XM_006721181.1:c.27+1G>A	XP_006721244.1:n.27+1G>A
XM_006721184.2:c.-72+1G>A	XP_006721247.1:n.-72+1G>A
XM_011523051.1:c.226+1G>A	XP_011521353.1:n.226+1G>A
XM_011523051.3:c.226+1G>A	XP_011521353.1:n.226+1G>A
XM_011523052.1:c.226+1G>A	XP_011521354.1:n.226+1G>A
XM_011523053.1:c.226+1G>A	XP_011521355.1:n.226+1G>A
XM_011523053.2:c.226+1G>A	XP_011521355.1:n.226+1G>A
XM_011523054.1:c.27+1G>A	XP_011521356.1:n.27+1G>A
XM_011523054.2:c.27+1G>A	XP_011521356.1:n.27+1G>A
XM_011523055.1:c.27+1G>A	XP_011521357.1:n.27+1G>A
XM_011523055.2:c.27+1G>A	XP_011521357.1:n.27+1G>A
XM_011523056.1:c.-23+1G>A	XP_011521358.1:n.-23+1G>A
XM_011523056.2:c.-23+1G>A	XP_011521358.1:n.-23+1G>A
XM_011523057.1:c.226+1G>A	XP_011521359.1:n.226+1G>A
XM_011523057.2:c.226+1G>A	XP_011521359.1:n.226+1G>A
XM_017023182.2:c.226+1G>A	XP_016878671.1:n.226+1G>A
XM_017023183.1:c.226+1G>A	XP_016878672.1:n.226+1G>A
XM_017023184.1:c.226+1G>A	XP_016878673.1:n.226+1G>A
XM_017023185.1:c.226+1G>A	XP_016878674.1:n.226+1G>A
XM_017023186.1:c.226+1G>A	XP_016878675.1:n.226+1G>A
XM_017023187.1:c.226+1G>A	XP_016878676.1:n.226+1G>A
XM_024450244.1:c.27+1G>A	XP_024306012.1:n.27+1G>A