Canonical Allele Identifier: CA5576260

Gene: ANXA11

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80169007C>A , CM000672.2:g.80169007C>A	GRCh38
NC_000010.10:g.81928763C>A , CM000672.1:g.81928763C>A	GRCh37
NC_000010.9:g.81918743C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422982.8:c.523G>T MANE Select	ENSP00000404412.2:p.Gly175Trp
ENST00000265447.8:c.424G>T	ENSP00000265447.5:p.Gly142Trp
ENST00000372231.7:c.523G>T	ENSP00000361305.3:p.Gly175Trp
ENST00000422982.7:c.523G>T	ENSP00000404412.2:p.Gly175Trp
ENST00000438331.5:c.523G>T	ENSP00000398610.1:p.Gly175Trp
ENST00000481805.1:n.81G>T
NM_001157.2:c.523G>T	NP_001148.1:p.Gly175Trp
NM_001278407.1:c.523G>T	NP_001265336.1:p.Gly175Trp
NM_001278408.1:c.523G>T	NP_001265337.1:p.Gly175Trp
NM_001278409.1:c.424G>T	NP_001265338.1:p.Gly142Trp
NM_145868.1:c.523G>T	NP_665875.1:p.Gly175Trp
NM_145869.1:c.523G>T	NP_665876.1:p.Gly175Trp
XM_005269741.3:c.823G>T	XP_005269798.1:p.Gly275Trp
XM_005269742.1:c.523G>T	XP_005269799.1:p.Gly175Trp
XM_006717813.1:c.523G>T	XP_006717876.1:p.Gly175Trp
XM_006717814.2:c.523G>T	XP_006717877.1:p.Gly175Trp
XM_011539735.1:c.523G>T	XP_011538037.1:p.Gly175Trp
XM_011539736.1:c.523G>T	XP_011538038.1:p.Gly175Trp
XM_005269741.4:c.823G>T	XP_005269798.1:p.Gly275Trp
XM_006717813.2:c.523G>T	XP_006717876.1:p.Gly175Trp
XM_011539736.3:c.523G>T	XP_011538038.1:p.Gly175Trp
NM_145868.2:c.523G>T MANE Select	NP_665875.1:p.Gly175Trp
NM_001157.3:c.523G>T	NP_001148.1:p.Gly175Trp
NM_001278407.2:c.523G>T	NP_001265336.1:p.Gly175Trp
NM_001278409.2:c.424G>T	NP_001265338.1:p.Gly142Trp
NM_145869.2:c.523G>T	NP_665876.1:p.Gly175Trp
NM_001278408.2:c.523G>T	NP_001265337.1:p.Gly175Trp