Canonical Allele Identifier: CA497375697

Gene: ANKRD11

Linked Data

• MyVariant Identifiers: chr16:g.89351657A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89285249A>G , CM000678.2:g.89285249A>G	GRCh38
NC_000016.9:g.89351657A>G , CM000678.1:g.89351657A>G	GRCh37
NC_000016.8:g.87879158A>G	NCBI36
NG_032003.1:g.210313T>C
NG_032003.2:g.210313T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000301030.10:c.1293T>C MANE Select	ENSP00000301030.4:p.His431=
ENST00000330736.10:c.*1096T>C	ENSP00000330815.5:n.*1096T>C
ENST00000378330.7:c.1293T>C	ENSP00000367581.2:p.His431=
ENST00000568100.2:n.999T>C
ENST00000642443.1:c.918T>C	ENSP00000493644.1:p.His306=
ENST00000642600.1:c.1293T>C	ENSP00000495226.1:p.His431=
ENST00000644285.1:c.744+3279T>C	ENSP00000496476.1:n.744+3279T>C
ENST00000645212.1:n.3065T>C
ENST00000646345.1:n.1285T>C
ENST00000301030.8:c.1293T>C	ENSP00000301030.4:p.His431=
ENST00000330736.9:c.*1096T>C	ENSP00000330815.5:n.*1096T>C
ENST00000378330.6:c.1293T>C	ENSP00000367581.2:p.His431=
ENST00000562194.1:c.151+3279T>C
ENST00000568100.1:n.844T>C
ENST00000613312.4:c.*191T>C	ENSP00000478018.1:n.*191T>C
NM_001256182.1:c.1293T>C	NP_001243111.1:p.His431=
NM_001256183.1:c.1293T>C	NP_001243112.1:p.His431=
NM_013275.5:c.1293T>C	NP_037407.4:p.His431=
XM_006721181.1:c.1191T>C	XP_006721244.1:p.His397=
XM_006721184.2:c.996T>C	XP_006721247.1:p.His332=
XM_011523051.1:c.1293T>C	XP_011521353.1:p.His431=
XM_011523052.1:c.1293T>C	XP_011521354.1:p.His431=
XM_011523053.1:c.1293T>C	XP_011521355.1:p.His431=
XM_011523054.1:c.1191T>C	XP_011521356.1:p.His397=
XM_011523055.1:c.1191T>C	XP_011521357.1:p.His397=
XM_011523056.1:c.1164T>C	XP_011521358.1:p.His388=
XM_011523057.1:c.1293T>C	XP_011521359.1:p.His431=
XM_011523051.3:c.1293T>C	XP_011521353.1:p.His431=
XM_011523053.2:c.1293T>C	XP_011521355.1:p.His431=
XM_011523054.2:c.1191T>C	XP_011521356.1:p.His397=
XM_011523055.2:c.1191T>C	XP_011521357.1:p.His397=
XM_011523056.2:c.1164T>C	XP_011521358.1:p.His388=
XM_011523057.2:c.1293T>C	XP_011521359.1:p.His431=
XM_017023182.2:c.1293T>C	XP_016878671.1:p.His431=
XM_017023183.1:c.1293T>C	XP_016878672.1:p.His431=
XM_017023184.1:c.1293T>C	XP_016878673.1:p.His431=
XM_017023185.1:c.1293T>C	XP_016878674.1:p.His431=
XM_017023186.1:c.1293T>C	XP_016878675.1:p.His431=
XM_017023187.1:c.1293T>C	XP_016878676.1:p.His431=
XM_024450244.1:c.1191T>C	XP_024306012.1:p.His397=
NM_013275.6:c.1293T>C MANE Select	NP_037407.4:p.His431=
NM_001256182.2:c.1293T>C	NP_001243111.1:p.His431=
NM_001256183.2:c.1293T>C	NP_001243112.1:p.His431=