Canonical Allele Identifier: CA1922520120

Gene: ANXA11

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80153805C= , CM000672.2:g.80153805C=	GRCh38
NC_000010.10:g.81913561C= , CM000672.1:g.81913561C=	GRCh37
NC_000010.9:g.81903541C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_145868.2:c.*2048G= MANE Select	NP_665875.1:n.*2048G=
ENST00000422982.8:c.*2048G= MANE Select	ENSP00000404412.2:n.*2048G=
NM_001157.3:c.*2048G=	NP_001148.1:n.*2048G=
NM_001278407.2:c.*2048G=	NP_001265336.1:n.*2048G=
NM_001278408.2:c.*2048G=	NP_001265337.1:n.*2048G=
NM_001278409.2:c.*2048G=	NP_001265338.1:n.*2048G=
NM_145869.2:c.*2048G=	NP_665876.1:n.*2048G=
ENST00000372231.7:c.*2048G=	ENSP00000361305.3:n.*2048G=
ENST00000438331.5:c.*2048G=	ENSP00000398610.1:n.*2048G=
XM_005269741.3:c.*2048G=	XP_005269798.1:n.*2048G=
XM_011539736.1:c.*2048G=	XP_011538038.1:n.*2048G=