Canonical Allele Identifier: CA397165274

Gene: ANKRD11

Linked Data

• MyVariant Identifiers: chr16:g.89351659G>C (hg19) ; chr16:g.89285251G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89285251G>C , CM000678.2:g.89285251G>C	GRCh38
NC_000016.9:g.89351659G>C , CM000678.1:g.89351659G>C	GRCh37
NC_000016.8:g.87879160G>C	NCBI36
NG_032003.1:g.210311C>G
NG_032003.2:g.210311C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000301030.10:c.1291C>G MANE Select	ENSP00000301030.4:p.His431Asp
ENST00000330736.10:c.*1094C>G	ENSP00000330815.5:n.*1094C>G
ENST00000378330.7:c.1291C>G	ENSP00000367581.2:p.His431Asp
ENST00000568100.2:n.997C>G
ENST00000642443.1:c.916C>G	ENSP00000493644.1:p.His306Asp
ENST00000642600.1:c.1291C>G	ENSP00000495226.1:p.His431Asp
ENST00000644285.1:c.744+3277C>G	ENSP00000496476.1:n.744+3277C>G
ENST00000645212.1:n.3063C>G
ENST00000646345.1:n.1283C>G
ENST00000301030.8:c.1291C>G	ENSP00000301030.4:p.His431Asp
ENST00000330736.9:c.*1094C>G	ENSP00000330815.5:n.*1094C>G
ENST00000378330.6:c.1291C>G	ENSP00000367581.2:p.His431Asp
ENST00000562194.1:c.151+3277C>G
ENST00000568100.1:n.842C>G
ENST00000613312.4:c.*189C>G	ENSP00000478018.1:n.*189C>G
NM_001256182.1:c.1291C>G	NP_001243111.1:p.His431Asp
NM_001256183.1:c.1291C>G	NP_001243112.1:p.His431Asp
NM_013275.5:c.1291C>G	NP_037407.4:p.His431Asp
XM_006721181.1:c.1189C>G	XP_006721244.1:p.His397Asp
XM_006721184.2:c.994C>G	XP_006721247.1:p.His332Asp
XM_011523051.1:c.1291C>G	XP_011521353.1:p.His431Asp
XM_011523052.1:c.1291C>G	XP_011521354.1:p.His431Asp
XM_011523053.1:c.1291C>G	XP_011521355.1:p.His431Asp
XM_011523054.1:c.1189C>G	XP_011521356.1:p.His397Asp
XM_011523055.1:c.1189C>G	XP_011521357.1:p.His397Asp
XM_011523056.1:c.1162C>G	XP_011521358.1:p.His388Asp
XM_011523057.1:c.1291C>G	XP_011521359.1:p.His431Asp
XM_011523051.3:c.1291C>G	XP_011521353.1:p.His431Asp
XM_011523053.2:c.1291C>G	XP_011521355.1:p.His431Asp
XM_011523054.2:c.1189C>G	XP_011521356.1:p.His397Asp
XM_011523055.2:c.1189C>G	XP_011521357.1:p.His397Asp
XM_011523056.2:c.1162C>G	XP_011521358.1:p.His388Asp
XM_011523057.2:c.1291C>G	XP_011521359.1:p.His431Asp
XM_017023182.2:c.1291C>G	XP_016878671.1:p.His431Asp
XM_017023183.1:c.1291C>G	XP_016878672.1:p.His431Asp
XM_017023184.1:c.1291C>G	XP_016878673.1:p.His431Asp
XM_017023185.1:c.1291C>G	XP_016878674.1:p.His431Asp
XM_017023186.1:c.1291C>G	XP_016878675.1:p.His431Asp
XM_017023187.1:c.1291C>G	XP_016878676.1:p.His431Asp
XM_024450244.1:c.1189C>G	XP_024306012.1:p.His397Asp
NM_013275.6:c.1291C>G MANE Select	NP_037407.4:p.His431Asp
NM_001256182.2:c.1291C>G	NP_001243111.1:p.His431Asp
NM_001256183.2:c.1291C>G	NP_001243112.1:p.His431Asp