Canonical Allele Identifier: CA286504550

Gene: ANKRD11

Linked Data

• ClinVar Variation Id: 1198644
• ClinVar RCV Id: RCV001562868
• dbSNP Id: rs5818705
• gnomAD v2: 16-89337145-CA-C
• gnomAD v3: 16-89270737-CA-C
• gnomAD v4: 16-89270737-CA-C
• MyVariant Identifiers: chr16:g.89337146del (hg19) ; chr16:g.89270738del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89270740del , CM000678.2:g.89270740del	GRCh38
NC_000016.9:g.89337148del , CM000678.1:g.89337148del	GRCh37
NC_000016.8:g.87864649del	NCBI36
NG_032003.1:g.224824del
NG_032003.2:g.224824del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301030.10:c.7806+79del MANE Select	ENSP00000301030.4:n.7806+79del
ENST00000330736.10:c.*7609+79del	ENSP00000330815.5:n.*7609+79del
ENST00000378330.7:c.7806+79del	ENSP00000367581.2:n.7806+79del
ENST00000642600.1:c.7806+79del	ENSP00000495226.1:n.7806+79del
ENST00000644285.1:c.1080+79del	ENSP00000496476.1:n.1080+79del
ENST00000301030.8:c.7806+79del	ENSP00000301030.4:n.7806+79del
ENST00000330736.9:c.*7609+79del	ENSP00000330815.5:n.*7609+79del
ENST00000378330.6:c.7806+79del	ENSP00000367581.2:n.7806+79del
ENST00000562194.1:c.487+79del
NM_001256182.1:c.7806+79del	NP_001243111.1:n.7806+79del
NM_001256183.1:c.7806+79del	NP_001243112.1:n.7806+79del
NM_013275.5:c.7806+79del	NP_037407.4:n.7806+79del
XM_006721181.1:c.7704+79del	XP_006721244.1:n.7704+79del
XM_006721184.2:c.7509+79del	XP_006721247.1:n.7509+79del
XM_011523051.1:c.7806+79del	XP_011521353.1:n.7806+79del
XM_011523052.1:c.7806+79del	XP_011521354.1:n.7806+79del
XM_011523053.1:c.7806+79del	XP_011521355.1:n.7806+79del
XM_011523054.1:c.7704+79del	XP_011521356.1:n.7704+79del
XM_011523055.1:c.7704+79del	XP_011521357.1:n.7704+79del
XM_011523056.1:c.7677+79del	XP_011521358.1:n.7677+79del
XM_011523057.1:c.7806+79del	XP_011521359.1:n.7806+79del
XM_011523051.3:c.7806+79del	XP_011521353.1:n.7806+79del
XM_011523053.2:c.7806+79del	XP_011521355.1:n.7806+79del
XM_011523054.2:c.7704+79del	XP_011521356.1:n.7704+79del
XM_011523055.2:c.7704+79del	XP_011521357.1:n.7704+79del
XM_011523056.2:c.7677+79del	XP_011521358.1:n.7677+79del
XM_011523057.2:c.7806+79del	XP_011521359.1:n.7806+79del
XM_017023182.2:c.7806+79del	XP_016878671.1:n.7806+79del
XM_017023183.1:c.7806+79del	XP_016878672.1:n.7806+79del
XM_017023184.1:c.7806+79del	XP_016878673.1:n.7806+79del
XM_017023185.1:c.7806+79del	XP_016878674.1:n.7806+79del
XM_017023186.1:c.7806+79del	XP_016878675.1:n.7806+79del
XM_017023187.1:c.7806+79del	XP_016878676.1:n.7806+79del
XM_024450244.1:c.7704+79del	XP_024306012.1:n.7704+79del
NM_013275.6:c.7806+79del MANE Select	NP_037407.4:n.7806+79del
NM_001256182.2:c.7806+79del	NP_001243111.1:n.7806+79del
NM_001256183.2:c.7806+79del	NP_001243112.1:n.7806+79del