Canonical Allele Identifier: CA8242812

Gene: ANKRD11

Linked Data

• ClinVar Variation Id: 2852666
• ClinVar RCV Id: RCV003640451
• dbSNP Id: rs148472572
• ExAC: 16:89351655 G / A
• gnomAD v2: 16-89351655-G-A
• gnomAD v3: 16-89285247-G-A
• gnomAD v4: 16-89285247-G-A
• MyVariant Identifiers: chr16:g.89351655G>A (hg19) ; chr16:g.89285247G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89285247G>A , CM000678.2:g.89285247G>A	GRCh38
NC_000016.9:g.89351655G>A , CM000678.1:g.89351655G>A	GRCh37
NC_000016.8:g.87879156G>A	NCBI36
NG_032003.1:g.210315C>T
NG_032003.2:g.210315C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000301030.10:c.1295C>T MANE Select	ENSP00000301030.4:p.Thr432Met
ENST00000330736.10:c.*1098C>T	ENSP00000330815.5:n.*1098C>T
ENST00000378330.7:c.1295C>T	ENSP00000367581.2:p.Thr432Met
ENST00000568100.2:n.1001C>T
ENST00000642443.1:c.920C>T	ENSP00000493644.1:p.Thr307Met
ENST00000642600.1:c.1295C>T	ENSP00000495226.1:p.Thr432Met
ENST00000644285.1:c.744+3281C>T	ENSP00000496476.1:n.744+3281C>T
ENST00000645212.1:n.3067C>T
ENST00000646345.1:n.1287C>T
ENST00000301030.8:c.1295C>T	ENSP00000301030.4:p.Thr432Met
ENST00000330736.9:c.*1098C>T	ENSP00000330815.5:n.*1098C>T
ENST00000378330.6:c.1295C>T	ENSP00000367581.2:p.Thr432Met
ENST00000562194.1:c.151+3281C>T
ENST00000568100.1:n.846C>T
ENST00000613312.4:c.*193C>T	ENSP00000478018.1:n.*193C>T
NM_001256182.1:c.1295C>T	NP_001243111.1:p.Thr432Met
NM_001256183.1:c.1295C>T	NP_001243112.1:p.Thr432Met
NM_013275.5:c.1295C>T	NP_037407.4:p.Thr432Met
XM_006721181.1:c.1193C>T	XP_006721244.1:p.Thr398Met
XM_006721184.2:c.998C>T	XP_006721247.1:p.Thr333Met
XM_011523051.1:c.1295C>T	XP_011521353.1:p.Thr432Met
XM_011523052.1:c.1295C>T	XP_011521354.1:p.Thr432Met
XM_011523053.1:c.1295C>T	XP_011521355.1:p.Thr432Met
XM_011523054.1:c.1193C>T	XP_011521356.1:p.Thr398Met
XM_011523055.1:c.1193C>T	XP_011521357.1:p.Thr398Met
XM_011523056.1:c.1166C>T	XP_011521358.1:p.Thr389Met
XM_011523057.1:c.1295C>T	XP_011521359.1:p.Thr432Met
XM_011523051.3:c.1295C>T	XP_011521353.1:p.Thr432Met
XM_011523053.2:c.1295C>T	XP_011521355.1:p.Thr432Met
XM_011523054.2:c.1193C>T	XP_011521356.1:p.Thr398Met
XM_011523055.2:c.1193C>T	XP_011521357.1:p.Thr398Met
XM_011523056.2:c.1166C>T	XP_011521358.1:p.Thr389Met
XM_011523057.2:c.1295C>T	XP_011521359.1:p.Thr432Met
XM_017023182.2:c.1295C>T	XP_016878671.1:p.Thr432Met
XM_017023183.1:c.1295C>T	XP_016878672.1:p.Thr432Met
XM_017023184.1:c.1295C>T	XP_016878673.1:p.Thr432Met
XM_017023185.1:c.1295C>T	XP_016878674.1:p.Thr432Met
XM_017023186.1:c.1295C>T	XP_016878675.1:p.Thr432Met
XM_017023187.1:c.1295C>T	XP_016878676.1:p.Thr432Met
XM_024450244.1:c.1193C>T	XP_024306012.1:p.Thr398Met
NM_013275.6:c.1295C>T MANE Select	NP_037407.4:p.Thr432Met
NM_001256182.2:c.1295C>T	NP_001243111.1:p.Thr432Met
NM_001256183.2:c.1295C>T	NP_001243112.1:p.Thr432Met