Canonical Allele Identifier: CA2241596183
Gene: ANKRD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89270844G= , CM000678.2:g.89270844G= GRCh38
NC_000016.9:g.89337252G= , CM000678.1:g.89337252G= GRCh37
NC_000016.8:g.87864753G= NCBI36
NG_032003.1:g.224718C=
NG_032003.2:g.224718C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301030.10:c.7779C= MANE Select ENSP00000301030.4:p.Asp2593=
ENST00000330736.10:c.*7582C= ENSP00000330815.5:n.*7582C=
ENST00000378330.7:c.7779C= ENSP00000367581.2:p.Asp2593=
ENST00000642600.1:c.7779C= ENSP00000495226.1:p.Asp2593=
ENST00000644285.1:c.1053C= ENSP00000496476.1:p.Asp351=
ENST00000301030.8:c.7779C= ENSP00000301030.4:p.Asp2593=
ENST00000330736.9:c.*7582C= ENSP00000330815.5:n.*7582C=
ENST00000378330.6:c.7779C= ENSP00000367581.2:p.Asp2593=
ENST00000562194.1:c.460C=
NM_001256182.1:c.7779C= NP_001243111.1:p.Asp2593=
NM_001256183.1:c.7779C= NP_001243112.1:p.Asp2593=
NM_013275.5:c.7779C= NP_037407.4:p.Asp2593=
XM_006721181.1:c.7677C= XP_006721244.1:p.Asp2559=
XM_006721184.2:c.7482C= XP_006721247.1:p.Asp2494=
XM_011523051.1:c.7779C= XP_011521353.1:p.Asp2593=
XM_011523052.1:c.7779C= XP_011521354.1:p.Asp2593=
XM_011523053.1:c.7779C= XP_011521355.1:p.Asp2593=
XM_011523054.1:c.7677C= XP_011521356.1:p.Asp2559=
XM_011523055.1:c.7677C= XP_011521357.1:p.Asp2559=
XM_011523056.1:c.7650C= XP_011521358.1:p.Asp2550=
XM_011523057.1:c.7779C= XP_011521359.1:p.Asp2593=
XM_011523051.3:c.7779C= XP_011521353.1:p.Asp2593=
XM_011523053.2:c.7779C= XP_011521355.1:p.Asp2593=
XM_011523054.2:c.7677C= XP_011521356.1:p.Asp2559=
XM_011523055.2:c.7677C= XP_011521357.1:p.Asp2559=
XM_011523056.2:c.7650C= XP_011521358.1:p.Asp2550=
XM_011523057.2:c.7779C= XP_011521359.1:p.Asp2593=
XM_017023182.2:c.7779C= XP_016878671.1:p.Asp2593=
XM_017023183.1:c.7779C= XP_016878672.1:p.Asp2593=
XM_017023184.1:c.7779C= XP_016878673.1:p.Asp2593=
XM_017023185.1:c.7779C= XP_016878674.1:p.Asp2593=
XM_017023186.1:c.7779C= XP_016878675.1:p.Asp2593=
XM_017023187.1:c.7779C= XP_016878676.1:p.Asp2593=
XM_024450244.1:c.7677C= XP_024306012.1:p.Asp2559=
NM_013275.6:c.7779C= MANE Select NP_037407.4:p.Asp2593=
NM_001256182.2:c.7779C= NP_001243111.1:p.Asp2593=
NM_001256183.2:c.7779C= NP_001243112.1:p.Asp2593=