Canonical Allele Identifier: CA930380139

Gene: ANXA11

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80201955C>T , CM000672.2:g.80201955C>T	GRCh38
NC_000010.10:g.81961711C>T , CM000672.1:g.81961711C>T	GRCh37
NC_000010.9:g.81951691C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422982.8:c.-58+3388G>A MANE Select	ENSP00000404412.2:n.-58+3388G>A
ENST00000372231.7:c.-9+3388G>A	ENSP00000361305.3:n.-9+3388G>A
ENST00000422982.7:c.-58+3388G>A	ENSP00000404412.2:n.-58+3388G>A
ENST00000438331.5:c.-254+3388G>A	ENSP00000398610.1:n.-254+3388G>A
ENST00000463657.1:n.180+3388G>A
ENST00000474545.1:n.94+2871G>A
NM_001157.2:c.-9+3388G>A	NP_001148.1:n.-9+3388G>A
NM_001278407.1:c.-58+3388G>A	NP_001265336.1:n.-58+3388G>A
NM_001278408.1:c.-573+2284G>A	NP_001265337.1:n.-573+2284G>A
NM_001278409.1:c.-426+3388G>A	NP_001265338.1:n.-426+3388G>A
NM_145868.1:c.-58+3388G>A	NP_665875.1:n.-58+3388G>A
NM_145869.1:c.-254+3388G>A	NP_665876.1:n.-254+3388G>A
XM_005269742.1:c.-9+3388G>A	XP_005269799.1:n.-9+3388G>A
XM_006717813.1:c.-58+3388G>A	XP_006717876.1:n.-58+3388G>A
XM_011539735.1:c.-573+3388G>A	XP_011538037.1:n.-573+3388G>A
XM_011539736.1:c.-573+3388G>A	XP_011538038.1:n.-573+3388G>A
XM_006717813.2:c.-58+3388G>A	XP_006717876.1:n.-58+3388G>A
XM_011539736.3:c.-573+3388G>A	XP_011538038.1:n.-573+3388G>A
NM_145868.2:c.-58+3388G>A MANE Select	NP_665875.1:n.-58+3388G>A
NM_001157.3:c.-9+3388G>A	NP_001148.1:n.-9+3388G>A
NM_001278407.2:c.-58+3388G>A	NP_001265336.1:n.-58+3388G>A
NM_001278409.2:c.-426+3388G>A	NP_001265338.1:n.-426+3388G>A
NM_145869.2:c.-254+3388G>A	NP_665876.1:n.-254+3388G>A
NM_001278408.2:c.-573+2284G>A	NP_001265337.1:n.-573+2284G>A