Canonical Allele Identifier: CA397167325

Gene: ANKRD11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89290730C>A , CM000678.2:g.89290730C>A	GRCh38
NC_000016.9:g.89357138C>A , CM000678.1:g.89357138C>A	GRCh37
NC_000016.8:g.87884639C>A	NCBI36
NG_032003.1:g.204832G>T
NG_032003.2:g.204832G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_013275.6:c.496G>T MANE Select	NP_037407.4:p.Glu166Ter
ENST00000301030.10:c.496G>T MANE Select	ENSP00000301030.4:p.Glu166Ter
NM_001256182.1:c.496G>T	NP_001243111.1:p.Glu166Ter
NM_001256182.2:c.496G>T	NP_001243111.1:p.Glu166Ter
NM_001256183.1:c.496G>T	NP_001243112.1:p.Glu166Ter
NM_001256183.2:c.496G>T	NP_001243112.1:p.Glu166Ter
NM_013275.5:c.496G>T	NP_037407.4:p.Glu166Ter
NR_045839.1:n.1327G>T
NR_045839.2:n.1327G>T
ENST00000301030.8:c.496G>T	ENSP00000301030.4:p.Glu166Ter
ENST00000330736.10:c.*299G>T	ENSP00000330815.5:n.*299G>T
ENST00000330736.9:c.*299G>T	ENSP00000330815.5:n.*299G>T
ENST00000378330.6:c.496G>T	ENSP00000367581.2:p.Glu166Ter
ENST00000378330.7:c.496G>T	ENSP00000367581.2:p.Glu166Ter
ENST00000378332.6:c.*758G>T	ENSP00000367583.2:n.*758G>T
ENST00000378332.7:c.*758G>T	ENSP00000367583.2:n.*758G>T
ENST00000562275.5:c.*299G>T	ENSP00000454550.1:n.*299G>T
ENST00000562275.6:c.*299G>T	ENSP00000454550.1:n.*299G>T
ENST00000567699.2:n.444-4544G>T
ENST00000613312.4:c.496G>T	ENSP00000478018.1:p.Glu166Ter
ENST00000642333.1:c.496G>T	ENSP00000496651.1:p.Glu166Ter
ENST00000642443.1:c.227-2060G>T	ENSP00000493644.1:n.227-2060G>T
ENST00000642600.1:c.496G>T	ENSP00000495226.1:p.Glu166Ter
ENST00000642695.1:c.496G>T	ENSP00000495449.1:p.Glu166Ter
ENST00000643964.1:c.*299G>T	ENSP00000495181.1:n.*299G>T
ENST00000644285.1:c.496G>T	ENSP00000496476.1:p.Glu166Ter
ENST00000644784.1:c.496G>T	ENSP00000496419.1:p.Glu166Ter
ENST00000645278.1:c.*126G>T	ENSP00000494850.1:n.*126G>T
ENST00000646345.1:n.488G>T
ENST00000646838.1:c.496G>T	ENSP00000495124.1:p.Glu166Ter
ENST00000646975.1:c.496G>T	ENSP00000495608.1:p.Glu166Ter
XM_006721181.1:c.394G>T	XP_006721244.1:p.Glu132Ter
XM_006721184.2:c.199G>T	XP_006721247.1:p.Glu67Ter
XM_011523051.1:c.496G>T	XP_011521353.1:p.Glu166Ter
XM_011523051.3:c.496G>T	XP_011521353.1:p.Glu166Ter
XM_011523052.1:c.496G>T	XP_011521354.1:p.Glu166Ter
XM_011523053.1:c.496G>T	XP_011521355.1:p.Glu166Ter
XM_011523053.2:c.496G>T	XP_011521355.1:p.Glu166Ter
XM_011523054.1:c.394G>T	XP_011521356.1:p.Glu132Ter
XM_011523054.2:c.394G>T	XP_011521356.1:p.Glu132Ter
XM_011523055.1:c.394G>T	XP_011521357.1:p.Glu132Ter
XM_011523055.2:c.394G>T	XP_011521357.1:p.Glu132Ter
XM_011523056.1:c.367G>T	XP_011521358.1:p.Glu123Ter
XM_011523056.2:c.367G>T	XP_011521358.1:p.Glu123Ter
XM_011523057.1:c.496G>T	XP_011521359.1:p.Glu166Ter
XM_011523057.2:c.496G>T	XP_011521359.1:p.Glu166Ter
XM_017023182.2:c.496G>T	XP_016878671.1:p.Glu166Ter
XM_017023183.1:c.496G>T	XP_016878672.1:p.Glu166Ter
XM_017023184.1:c.496G>T	XP_016878673.1:p.Glu166Ter
XM_017023185.1:c.496G>T	XP_016878674.1:p.Glu166Ter
XM_017023186.1:c.496G>T	XP_016878675.1:p.Glu166Ter
XM_017023187.1:c.496G>T	XP_016878676.1:p.Glu166Ter
XM_024450244.1:c.394G>T	XP_024306012.1:p.Glu132Ter