Canonical Allele Identifier: CA279648

Gene: ANKRD11

Linked Data

• ClinVar Variation Id: 217881
• ClinVar RCV Id: RCV000201945 ; RCV000989659
• dbSNP Id: rs863225296
• MyVariant Identifiers: chr16:g.89345770G>A (hg19) ; chr16:g.89279362G>A (hg38)
• PubMed: PMID:21782149

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89279362G>A , CM000678.2:g.89279362G>A	GRCh38
NC_000016.9:g.89345770G>A , CM000678.1:g.89345770G>A	GRCh37
NC_000016.8:g.87873271G>A	NCBI36
NG_032003.1:g.216200C>T
NG_032003.2:g.216200C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000301030.10:c.7180C>T MANE Select	ENSP00000301030.4:p.Gln2394Ter
ENST00000330736.10:c.*6983C>T	ENSP00000330815.5:n.*6983C>T
ENST00000378330.7:c.7180C>T	ENSP00000367581.2:p.Gln2394Ter
ENST00000642600.1:c.7180C>T	ENSP00000495226.1:p.Gln2394Ter
ENST00000644285.1:c.745-4171C>T	ENSP00000496476.1:n.745-4171C>T
ENST00000301030.8:c.7180C>T	ENSP00000301030.4:p.Gln2394Ter
ENST00000330736.9:c.*6983C>T	ENSP00000330815.5:n.*6983C>T
ENST00000378330.6:c.7180C>T	ENSP00000367581.2:p.Gln2394Ter
ENST00000562194.1:c.152-4171C>T
ENST00000623388.1:n.355C>T
NM_001256182.1:c.7180C>T	NP_001243111.1:p.Gln2394Ter
NM_001256183.1:c.7180C>T	NP_001243112.1:p.Gln2394Ter
NM_013275.5:c.7180C>T	NP_037407.4:p.Gln2394Ter
XM_006721181.1:c.7078C>T	XP_006721244.1:p.Gln2360Ter
XM_006721184.2:c.6883C>T	XP_006721247.1:p.Gln2295Ter
XM_011523051.1:c.7180C>T	XP_011521353.1:p.Gln2394Ter
XM_011523052.1:c.7180C>T	XP_011521354.1:p.Gln2394Ter
XM_011523053.1:c.7180C>T	XP_011521355.1:p.Gln2394Ter
XM_011523054.1:c.7078C>T	XP_011521356.1:p.Gln2360Ter
XM_011523055.1:c.7078C>T	XP_011521357.1:p.Gln2360Ter
XM_011523056.1:c.7051C>T	XP_011521358.1:p.Gln2351Ter
XM_011523057.1:c.7180C>T	XP_011521359.1:p.Gln2394Ter
XM_011523051.3:c.7180C>T	XP_011521353.1:p.Gln2394Ter
XM_011523053.2:c.7180C>T	XP_011521355.1:p.Gln2394Ter
XM_011523054.2:c.7078C>T	XP_011521356.1:p.Gln2360Ter
XM_011523055.2:c.7078C>T	XP_011521357.1:p.Gln2360Ter
XM_011523056.2:c.7051C>T	XP_011521358.1:p.Gln2351Ter
XM_011523057.2:c.7180C>T	XP_011521359.1:p.Gln2394Ter
XM_017023182.2:c.7180C>T	XP_016878671.1:p.Gln2394Ter
XM_017023183.1:c.7180C>T	XP_016878672.1:p.Gln2394Ter
XM_017023184.1:c.7180C>T	XP_016878673.1:p.Gln2394Ter
XM_017023185.1:c.7180C>T	XP_016878674.1:p.Gln2394Ter
XM_017023186.1:c.7180C>T	XP_016878675.1:p.Gln2394Ter
XM_017023187.1:c.7180C>T	XP_016878676.1:p.Gln2394Ter
XM_024450244.1:c.7078C>T	XP_024306012.1:p.Gln2360Ter
NM_013275.6:c.7180C>T MANE Select	NP_037407.4:p.Gln2394Ter
NM_001256182.2:c.7180C>T	NP_001243111.1:p.Gln2394Ter
NM_001256183.2:c.7180C>T	NP_001243112.1:p.Gln2394Ter