Canonical Allele Identifier: CA470453000

Gene: ANXA11

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80161951C>T , CM000672.2:g.80161951C>T	GRCh38
NC_000010.10:g.81921707C>T , CM000672.1:g.81921707C>T	GRCh37
NC_000010.9:g.81911687C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_145868.2:c.1164G>A MANE Select	NP_665875.1:p.Arg388=
ENST00000422982.8:c.1164G>A MANE Select	ENSP00000404412.2:p.Arg388=
NM_001157.2:c.1164G>A	NP_001148.1:p.Arg388=
NM_001157.3:c.1164G>A	NP_001148.1:p.Arg388=
NM_001278407.1:c.1164G>A	NP_001265336.1:p.Arg388=
NM_001278407.2:c.1164G>A	NP_001265336.1:p.Arg388=
NM_001278408.1:c.1164G>A	NP_001265337.1:p.Arg388=
NM_001278408.2:c.1164G>A	NP_001265337.1:p.Arg388=
NM_001278409.1:c.1065G>A	NP_001265338.1:p.Arg355=
NM_001278409.2:c.1065G>A	NP_001265338.1:p.Arg355=
NM_145868.1:c.1164G>A	NP_665875.1:p.Arg388=
NM_145869.1:c.1164G>A	NP_665876.1:p.Arg388=
NM_145869.2:c.1164G>A	NP_665876.1:p.Arg388=
ENST00000265447.8:c.1065G>A	ENSP00000265447.5:p.Arg355=
ENST00000372231.7:c.1164G>A	ENSP00000361305.3:p.Arg388=
ENST00000422982.7:c.1164G>A	ENSP00000404412.2:p.Arg388=
ENST00000438331.5:c.1164G>A	ENSP00000398610.1:p.Arg388=
ENST00000447489.1:c.62G>A
XM_005269741.3:c.1464G>A	XP_005269798.1:p.Arg488=
XM_005269741.4:c.1464G>A	XP_005269798.1:p.Arg488=
XM_005269742.1:c.1164G>A	XP_005269799.1:p.Arg388=
XM_006717813.1:c.1164G>A	XP_006717876.1:p.Arg388=
XM_006717813.2:c.1164G>A	XP_006717876.1:p.Arg388=
XM_006717814.2:c.1164G>A	XP_006717877.1:p.Arg388=
XM_011539735.1:c.1164G>A	XP_011538037.1:p.Arg388=
XM_011539736.1:c.1164G>A	XP_011538038.1:p.Arg388=
XM_011539736.3:c.1164G>A	XP_011538038.1:p.Arg388=