Canonical Allele Identifier: CA2241587344

Gene: ANKRD11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89280344_89280345delinsGA , CM000678.2:g.89280344_89280345delinsGA	GRCh38
NC_000016.9:g.89346752_89346753delinsGA , CM000678.1:g.89346752_89346753delinsGA	GRCh37
NC_000016.8:g.87874253_87874254delinsGA	NCBI36
NG_032003.1:g.215217_215218delinsTC
NG_032003.2:g.215217_215218delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301030.10:c.6197_6198delinsTC MANE Select	ENSP00000301030.4:p.Phe2066=
ENST00000330736.10:c.*6000_*6001delinsTC	ENSP00000330815.5:n.*6000_*6001delinsTC
ENST00000378330.7:c.6197_6198delinsTC	ENSP00000367581.2:p.Phe2066=
ENST00000642600.1:c.6197_6198delinsTC	ENSP00000495226.1:p.Phe2066=
ENST00000644285.1:c.745-5154_745-5153delinsTC	ENSP00000496476.1:n.745-5154_745-5153delinsTC
ENST00000301030.8:c.6197_6198delinsTC	ENSP00000301030.4:p.Phe2066=
ENST00000330736.9:c.*6000_*6001delinsTC	ENSP00000330815.5:n.*6000_*6001delinsTC
ENST00000378330.6:c.6197_6198delinsTC	ENSP00000367581.2:p.Phe2066=
ENST00000562194.1:c.152-5154_152-5153delinsTC
NM_001256182.1:c.6197_6198delinsTC	NP_001243111.1:p.Phe2066=
NM_001256183.1:c.6197_6198delinsTC	NP_001243112.1:p.Phe2066=
NM_013275.5:c.6197_6198delinsTC	NP_037407.4:p.Phe2066=
XM_006721181.1:c.6095_6096delinsTC	XP_006721244.1:p.Phe2032=
XM_006721184.2:c.5900_5901delinsTC	XP_006721247.1:p.Phe1967=
XM_011523051.1:c.6197_6198delinsTC	XP_011521353.1:p.Phe2066=
XM_011523052.1:c.6197_6198delinsTC	XP_011521354.1:p.Phe2066=
XM_011523053.1:c.6197_6198delinsTC	XP_011521355.1:p.Phe2066=
XM_011523054.1:c.6095_6096delinsTC	XP_011521356.1:p.Phe2032=
XM_011523055.1:c.6095_6096delinsTC	XP_011521357.1:p.Phe2032=
XM_011523056.1:c.6068_6069delinsTC	XP_011521358.1:p.Phe2023=
XM_011523057.1:c.6197_6198delinsTC	XP_011521359.1:p.Phe2066=
XM_011523051.3:c.6197_6198delinsTC	XP_011521353.1:p.Phe2066=
XM_011523053.2:c.6197_6198delinsTC	XP_011521355.1:p.Phe2066=
XM_011523054.2:c.6095_6096delinsTC	XP_011521356.1:p.Phe2032=
XM_011523055.2:c.6095_6096delinsTC	XP_011521357.1:p.Phe2032=
XM_011523056.2:c.6068_6069delinsTC	XP_011521358.1:p.Phe2023=
XM_011523057.2:c.6197_6198delinsTC	XP_011521359.1:p.Phe2066=
XM_017023182.2:c.6197_6198delinsTC	XP_016878671.1:p.Phe2066=
XM_017023183.1:c.6197_6198delinsTC	XP_016878672.1:p.Phe2066=
XM_017023184.1:c.6197_6198delinsTC	XP_016878673.1:p.Phe2066=
XM_017023185.1:c.6197_6198delinsTC	XP_016878674.1:p.Phe2066=
XM_017023186.1:c.6197_6198delinsTC	XP_016878675.1:p.Phe2066=
XM_017023187.1:c.6197_6198delinsTC	XP_016878676.1:p.Phe2066=
XM_024450244.1:c.6095_6096delinsTC	XP_024306012.1:p.Phe2032=
NM_013275.6:c.6197_6198delinsTC MANE Select	NP_037407.4:p.Phe2066=
NM_001256182.2:c.6197_6198delinsTC	NP_001243111.1:p.Phe2066=
NM_001256183.2:c.6197_6198delinsTC	NP_001243112.1:p.Phe2066=