Canonical Allele Identifier: CA497375700

Gene: ANKRD11

Linked Data

• MyVariant Identifiers: chr16:g.89351660T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89285252T>A , CM000678.2:g.89285252T>A	GRCh38
NC_000016.9:g.89351660T>A , CM000678.1:g.89351660T>A	GRCh37
NC_000016.8:g.87879161T>A	NCBI36
NG_032003.1:g.210310A>T
NG_032003.2:g.210310A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000301030.10:c.1290A>T MANE Select	ENSP00000301030.4:p.Ala430=
ENST00000330736.10:c.*1093A>T	ENSP00000330815.5:n.*1093A>T
ENST00000378330.7:c.1290A>T	ENSP00000367581.2:p.Ala430=
ENST00000568100.2:n.996A>T
ENST00000642443.1:c.915A>T	ENSP00000493644.1:p.Ala305=
ENST00000642600.1:c.1290A>T	ENSP00000495226.1:p.Ala430=
ENST00000644285.1:c.744+3276A>T	ENSP00000496476.1:n.744+3276A>T
ENST00000645212.1:n.3062A>T
ENST00000646345.1:n.1282A>T
ENST00000301030.8:c.1290A>T	ENSP00000301030.4:p.Ala430=
ENST00000330736.9:c.*1093A>T	ENSP00000330815.5:n.*1093A>T
ENST00000378330.6:c.1290A>T	ENSP00000367581.2:p.Ala430=
ENST00000562194.1:c.151+3276A>T
ENST00000568100.1:n.841A>T
ENST00000613312.4:c.*188A>T	ENSP00000478018.1:n.*188A>T
NM_001256182.1:c.1290A>T	NP_001243111.1:p.Ala430=
NM_001256183.1:c.1290A>T	NP_001243112.1:p.Ala430=
NM_013275.5:c.1290A>T	NP_037407.4:p.Ala430=
XM_006721181.1:c.1188A>T	XP_006721244.1:p.Ala396=
XM_006721184.2:c.993A>T	XP_006721247.1:p.Ala331=
XM_011523051.1:c.1290A>T	XP_011521353.1:p.Ala430=
XM_011523052.1:c.1290A>T	XP_011521354.1:p.Ala430=
XM_011523053.1:c.1290A>T	XP_011521355.1:p.Ala430=
XM_011523054.1:c.1188A>T	XP_011521356.1:p.Ala396=
XM_011523055.1:c.1188A>T	XP_011521357.1:p.Ala396=
XM_011523056.1:c.1161A>T	XP_011521358.1:p.Ala387=
XM_011523057.1:c.1290A>T	XP_011521359.1:p.Ala430=
XM_011523051.3:c.1290A>T	XP_011521353.1:p.Ala430=
XM_011523053.2:c.1290A>T	XP_011521355.1:p.Ala430=
XM_011523054.2:c.1188A>T	XP_011521356.1:p.Ala396=
XM_011523055.2:c.1188A>T	XP_011521357.1:p.Ala396=
XM_011523056.2:c.1161A>T	XP_011521358.1:p.Ala387=
XM_011523057.2:c.1290A>T	XP_011521359.1:p.Ala430=
XM_017023182.2:c.1290A>T	XP_016878671.1:p.Ala430=
XM_017023183.1:c.1290A>T	XP_016878672.1:p.Ala430=
XM_017023184.1:c.1290A>T	XP_016878673.1:p.Ala430=
XM_017023185.1:c.1290A>T	XP_016878674.1:p.Ala430=
XM_017023186.1:c.1290A>T	XP_016878675.1:p.Ala430=
XM_017023187.1:c.1290A>T	XP_016878676.1:p.Ala430=
XM_024450244.1:c.1188A>T	XP_024306012.1:p.Ala396=
NM_013275.6:c.1290A>T MANE Select	NP_037407.4:p.Ala430=
NM_001256182.2:c.1290A>T	NP_001243111.1:p.Ala430=
NM_001256183.2:c.1290A>T	NP_001243112.1:p.Ala430=