Canonical Allele Identifier: CA13161894

Gene: ANXA11

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80151969C>T , CM000672.2:g.80151969C>T	GRCh38
NC_000010.10:g.81911725C>T , CM000672.1:g.81911725C>T	GRCh37
NC_000010.9:g.81901705C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422982.8:c.*3884G>A MANE Select	ENSP00000404412.2:n.*3884G>A
ENST00000372231.7:c.*3884G>A	ENSP00000361305.3:n.*3884G>A
ENST00000438331.5:c.*3884G>A	ENSP00000398610.1:n.*3884G>A
NM_145868.2:c.*3884G>A MANE Select	NP_665875.1:n.*3884G>A
NM_001157.3:c.*3884G>A	NP_001148.1:n.*3884G>A
NM_001278407.2:c.*3884G>A	NP_001265336.1:n.*3884G>A
NM_001278409.2:c.*3884G>A	NP_001265338.1:n.*3884G>A
NM_145869.2:c.*3884G>A	NP_665876.1:n.*3884G>A
NM_001278408.2:c.*3884G>A	NP_001265337.1:n.*3884G>A