Canonical Allele Identifier: CA1922529552

Gene: ANXA11

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80173928A= , CM000672.2:g.80173928A=	GRCh38
NC_000010.10:g.81933684A= , CM000672.1:g.81933684A=	GRCh37
NC_000010.9:g.81923664A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000422982.8:c.-8-1059T= MANE Select	ENSP00000404412.2:n.-8-1059T=
ENST00000372231.7:c.-8-1059T=	ENSP00000361305.3:n.-8-1059T=
ENST00000422982.7:c.-8-1059T=	ENSP00000404412.2:n.-8-1059T=
ENST00000438331.5:c.-8-1059T=	ENSP00000398610.1:n.-8-1059T=
ENST00000463657.1:n.745-1059T=
NM_001157.2:c.-8-1059T=	NP_001148.1:n.-8-1059T=
NM_001278407.1:c.-8-1059T=	NP_001265336.1:n.-8-1059T=
NM_001278408.1:c.-8-1059T=	NP_001265337.1:n.-8-1059T=
NM_001278409.1:c.-376-1059T=	NP_001265338.1:n.-376-1059T=
NM_145868.1:c.-8-1059T=	NP_665875.1:n.-8-1059T=
NM_145869.1:c.-8-1059T=	NP_665876.1:n.-8-1059T=
XM_005269742.1:c.-8-1059T=	XP_005269799.1:n.-8-1059T=
XM_006717813.1:c.-8-1059T=	XP_006717876.1:n.-8-1059T=
XM_006717814.2:c.-8-1059T=	XP_006717877.1:n.-8-1059T=
XM_011539735.1:c.-8-1059T=	XP_011538037.1:n.-8-1059T=
XM_011539736.1:c.-8-1059T=	XP_011538038.1:n.-8-1059T=
XM_006717813.2:c.-8-1059T=	XP_006717876.1:n.-8-1059T=
XM_011539736.3:c.-8-1059T=	XP_011538038.1:n.-8-1059T=
NM_145868.2:c.-8-1059T= MANE Select	NP_665875.1:n.-8-1059T=
NM_001157.3:c.-8-1059T=	NP_001148.1:n.-8-1059T=
NM_001278407.2:c.-8-1059T=	NP_001265336.1:n.-8-1059T=
NM_001278409.2:c.-376-1059T=	NP_001265338.1:n.-376-1059T=
NM_145869.2:c.-8-1059T=	NP_665876.1:n.-8-1059T=
NM_001278408.2:c.-8-1059T=	NP_001265337.1:n.-8-1059T=