Canonical Allele Identifier: CA286505945

Gene: ANKRD11

Linked Data

• ClinVar Variation Id: 1254226
• ClinVar RCV Id: RCV001653008
• dbSNP Id: rs753798424
• gnomAD v2: 16-89341582-G-A
• gnomAD v3: 16-89275174-G-A
• gnomAD v4: 16-89275174-G-A
• MyVariant Identifiers: chr16:g.89341582G>A (hg19) ; chr16:g.89275174G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89275174G>A , CM000678.2:g.89275174G>A	GRCh38
NC_000016.9:g.89341582G>A , CM000678.1:g.89341582G>A	GRCh37
NC_000016.8:g.87869083G>A	NCBI36
NG_032003.1:g.220388C>T
NG_032003.2:g.220388C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301030.10:c.7488C>T MANE Select	ENSP00000301030.4:p.Ser2496=
ENST00000330736.10:c.*7291C>T	ENSP00000330815.5:n.*7291C>T
ENST00000378330.7:c.7488C>T	ENSP00000367581.2:p.Ser2496=
ENST00000642600.1:c.7488C>T	ENSP00000495226.1:p.Ser2496=
ENST00000644285.1:c.762C>T	ENSP00000496476.1:p.Ser254=
ENST00000301030.8:c.7488C>T	ENSP00000301030.4:p.Ser2496=
ENST00000330736.9:c.*7291C>T	ENSP00000330815.5:n.*7291C>T
ENST00000378330.6:c.7488C>T	ENSP00000367581.2:p.Ser2496=
ENST00000562194.1:c.169C>T
NM_001256182.1:c.7488C>T	NP_001243111.1:p.Ser2496=
NM_001256183.1:c.7488C>T	NP_001243112.1:p.Ser2496=
NM_013275.5:c.7488C>T	NP_037407.4:p.Ser2496=
XM_006721181.1:c.7386C>T	XP_006721244.1:p.Ser2462=
XM_006721184.2:c.7191C>T	XP_006721247.1:p.Ser2397=
XM_011523051.1:c.7488C>T	XP_011521353.1:p.Ser2496=
XM_011523052.1:c.7488C>T	XP_011521354.1:p.Ser2496=
XM_011523053.1:c.7488C>T	XP_011521355.1:p.Ser2496=
XM_011523054.1:c.7386C>T	XP_011521356.1:p.Ser2462=
XM_011523055.1:c.7386C>T	XP_011521357.1:p.Ser2462=
XM_011523056.1:c.7359C>T	XP_011521358.1:p.Ser2453=
XM_011523057.1:c.7488C>T	XP_011521359.1:p.Ser2496=
XM_011523051.3:c.7488C>T	XP_011521353.1:p.Ser2496=
XM_011523053.2:c.7488C>T	XP_011521355.1:p.Ser2496=
XM_011523054.2:c.7386C>T	XP_011521356.1:p.Ser2462=
XM_011523055.2:c.7386C>T	XP_011521357.1:p.Ser2462=
XM_011523056.2:c.7359C>T	XP_011521358.1:p.Ser2453=
XM_011523057.2:c.7488C>T	XP_011521359.1:p.Ser2496=
XM_017023182.2:c.7488C>T	XP_016878671.1:p.Ser2496=
XM_017023183.1:c.7488C>T	XP_016878672.1:p.Ser2496=
XM_017023184.1:c.7488C>T	XP_016878673.1:p.Ser2496=
XM_017023185.1:c.7488C>T	XP_016878674.1:p.Ser2496=
XM_017023186.1:c.7488C>T	XP_016878675.1:p.Ser2496=
XM_017023187.1:c.7488C>T	XP_016878676.1:p.Ser2496=
XM_024450244.1:c.7386C>T	XP_024306012.1:p.Ser2462=
NM_013275.6:c.7488C>T MANE Select	NP_037407.4:p.Ser2496=
NM_001256182.2:c.7488C>T	NP_001243111.1:p.Ser2496=
NM_001256183.2:c.7488C>T	NP_001243112.1:p.Ser2496=