Canonical Allele Identifier: CA1922522910
Gene: ANXA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80160044T>A , CM000672.2:g.80160044T>A GRCh38
NC_000010.10:g.81919800T>A , CM000672.1:g.81919800T>A GRCh37
NC_000010.9:g.81909780T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000422982.8:c.1181-849A>T MANE Select ENSP00000404412.2:n.1181-849A>T
ENST00000265447.8:c.1082-849A>T ENSP00000265447.5:n.1082-849A>T
ENST00000372231.7:c.1181-849A>T ENSP00000361305.3:n.1181-849A>T
ENST00000422982.7:c.1181-849A>T ENSP00000404412.2:n.1181-849A>T
ENST00000438331.5:c.1181-849A>T ENSP00000398610.1:n.1181-849A>T
ENST00000447489.1:c.79-849A>T
NM_001157.2:c.1181-849A>T NP_001148.1:n.1181-849A>T
NM_001278407.1:c.1181-849A>T NP_001265336.1:n.1181-849A>T
NM_001278408.1:c.1181-849A>T NP_001265337.1:n.1181-849A>T
NM_001278409.1:c.1082-849A>T NP_001265338.1:n.1082-849A>T
NM_145868.1:c.1181-849A>T NP_665875.1:n.1181-849A>T
NM_145869.1:c.1181-849A>T NP_665876.1:n.1181-849A>T
XM_005269741.3:c.1481-849A>T XP_005269798.1:n.1481-849A>T
XM_005269742.1:c.1181-849A>T XP_005269799.1:n.1181-849A>T
XM_006717813.1:c.1181-849A>T XP_006717876.1:n.1181-849A>T
XM_006717814.2:c.1181-849A>T XP_006717877.1:n.1181-849A>T
XM_011539735.1:c.1181-849A>T XP_011538037.1:n.1181-849A>T
XM_011539736.1:c.1181-849A>T XP_011538038.1:n.1181-849A>T
XM_005269741.4:c.1481-849A>T XP_005269798.1:n.1481-849A>T
XM_006717813.2:c.1181-849A>T XP_006717876.1:n.1181-849A>T
XM_011539736.3:c.1181-849A>T XP_011538038.1:n.1181-849A>T
NM_145868.2:c.1181-849A>T MANE Select NP_665875.1:n.1181-849A>T
NM_001157.3:c.1181-849A>T NP_001148.1:n.1181-849A>T
NM_001278407.2:c.1181-849A>T NP_001265336.1:n.1181-849A>T
NM_001278409.2:c.1082-849A>T NP_001265338.1:n.1082-849A>T
NM_145869.2:c.1181-849A>T NP_665876.1:n.1181-849A>T
NM_001278408.2:c.1181-849A>T NP_001265337.1:n.1181-849A>T