Canonical Allele Identifier: CA2634942354

Gene: ANKRD11

Linked Data

• gnomAD v4: 16-89280145-GGTCCAGGTCGTCCTCGGGGCCGGCGAAGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89280150_89280179del , CM000678.2:g.89280150_89280179del	GRCh38
NC_000016.9:g.89346558_89346587del , CM000678.1:g.89346558_89346587del	GRCh37
NC_000016.8:g.87874059_87874088del	NCBI36
NG_032003.1:g.215387_215416del
NG_032003.2:g.215387_215416del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301030.10:c.6367_6396del MANE Select	ENSP00000301030.4:p.Ala2123_Asp2132del
ENST00000330736.10:c.*6170_*6199del	ENSP00000330815.5:n.*6170_*6199del
ENST00000378330.7:c.6367_6396del	ENSP00000367581.2:p.Ala2123_Asp2132del
ENST00000642600.1:c.6367_6396del	ENSP00000495226.1:p.Ala2123_Asp2132del
ENST00000644285.1:c.745-4984_745-4955del	ENSP00000496476.1:n.745-4984_745-4955del
ENST00000301030.8:c.6367_6396del	ENSP00000301030.4:p.Ala2123_Asp2132del
ENST00000330736.9:c.*6170_*6199del	ENSP00000330815.5:n.*6170_*6199del
ENST00000378330.6:c.6367_6396del	ENSP00000367581.2:p.Ala2123_Asp2132del
ENST00000562194.1:c.152-4984_152-4955del
NM_001256182.1:c.6367_6396del	NP_001243111.1:p.Ala2123_Asp2132del
NM_001256183.1:c.6367_6396del	NP_001243112.1:p.Ala2123_Asp2132del
NM_013275.5:c.6367_6396del	NP_037407.4:p.Ala2123_Asp2132del
XM_006721181.1:c.6265_6294del	XP_006721244.1:p.Ala2089_Asp2098del
XM_006721184.2:c.6070_6099del	XP_006721247.1:p.Ala2024_Asp2033del
XM_011523051.1:c.6367_6396del	XP_011521353.1:p.Ala2123_Asp2132del
XM_011523052.1:c.6367_6396del	XP_011521354.1:p.Ala2123_Asp2132del
XM_011523053.1:c.6367_6396del	XP_011521355.1:p.Ala2123_Asp2132del
XM_011523054.1:c.6265_6294del	XP_011521356.1:p.Ala2089_Asp2098del
XM_011523055.1:c.6265_6294del	XP_011521357.1:p.Ala2089_Asp2098del
XM_011523056.1:c.6238_6267del	XP_011521358.1:p.Ala2080_Asp2089del
XM_011523057.1:c.6367_6396del	XP_011521359.1:p.Ala2123_Asp2132del
XM_011523051.3:c.6367_6396del	XP_011521353.1:p.Ala2123_Asp2132del
XM_011523053.2:c.6367_6396del	XP_011521355.1:p.Ala2123_Asp2132del
XM_011523054.2:c.6265_6294del	XP_011521356.1:p.Ala2089_Asp2098del
XM_011523055.2:c.6265_6294del	XP_011521357.1:p.Ala2089_Asp2098del
XM_011523056.2:c.6238_6267del	XP_011521358.1:p.Ala2080_Asp2089del
XM_011523057.2:c.6367_6396del	XP_011521359.1:p.Ala2123_Asp2132del
XM_017023182.2:c.6367_6396del	XP_016878671.1:p.Ala2123_Asp2132del
XM_017023183.1:c.6367_6396del	XP_016878672.1:p.Ala2123_Asp2132del
XM_017023184.1:c.6367_6396del	XP_016878673.1:p.Ala2123_Asp2132del
XM_017023185.1:c.6367_6396del	XP_016878674.1:p.Ala2123_Asp2132del
XM_017023186.1:c.6367_6396del	XP_016878675.1:p.Ala2123_Asp2132del
XM_017023187.1:c.6367_6396del	XP_016878676.1:p.Ala2123_Asp2132del
XM_024450244.1:c.6265_6294del	XP_024306012.1:p.Ala2089_Asp2098del
NM_013275.6:c.6367_6396del MANE Select	NP_037407.4:p.Ala2123_Asp2132del
NM_001256182.2:c.6367_6396del	NP_001243111.1:p.Ala2123_Asp2132del
NM_001256183.2:c.6367_6396del	NP_001243112.1:p.Ala2123_Asp2132del