Canonical Allele Identifier: CA377368837

Gene: ANXA11

Linked Data

• MyVariant Identifiers: chr10:g.81930615C>G (hg19) ; chr10:g.80170859C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80170859C>G , CM000672.2:g.80170859C>G	GRCh38
NC_000010.10:g.81930615C>G , CM000672.1:g.81930615C>G	GRCh37
NC_000010.9:g.81920595C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422982.8:c.112G>C MANE Select	ENSP00000404412.2:p.Gly38Arg
ENST00000265447.8:c.13G>C	ENSP00000265447.5:p.Gly5Arg
ENST00000372231.7:c.112G>C	ENSP00000361305.3:p.Gly38Arg
ENST00000422982.7:c.112G>C	ENSP00000404412.2:p.Gly38Arg
ENST00000437799.1:c.112G>C	ENSP00000414642.1:p.Gly38Arg
ENST00000438331.5:c.112G>C	ENSP00000398610.1:p.Gly38Arg
NM_001157.2:c.112G>C	NP_001148.1:p.Gly38Arg
NM_001278407.1:c.112G>C	NP_001265336.1:p.Gly38Arg
NM_001278408.1:c.112G>C	NP_001265337.1:p.Gly38Arg
NM_001278409.1:c.13G>C	NP_001265338.1:p.Gly5Arg
NM_145868.1:c.112G>C	NP_665875.1:p.Gly38Arg
NM_145869.1:c.112G>C	NP_665876.1:p.Gly38Arg
XM_005269741.3:c.412G>C	XP_005269798.1:p.Gly138Arg
XM_005269742.1:c.112G>C	XP_005269799.1:p.Gly38Arg
XM_006717813.1:c.112G>C	XP_006717876.1:p.Gly38Arg
XM_006717814.2:c.112G>C	XP_006717877.1:p.Gly38Arg
XM_011539735.1:c.112G>C	XP_011538037.1:p.Gly38Arg
XM_011539736.1:c.112G>C	XP_011538038.1:p.Gly38Arg
XM_005269741.4:c.412G>C	XP_005269798.1:p.Gly138Arg
XM_006717813.2:c.112G>C	XP_006717876.1:p.Gly38Arg
XM_011539736.3:c.112G>C	XP_011538038.1:p.Gly38Arg
NM_145868.2:c.112G>C MANE Select	NP_665875.1:p.Gly38Arg
NM_001157.3:c.112G>C	NP_001148.1:p.Gly38Arg
NM_001278407.2:c.112G>C	NP_001265336.1:p.Gly38Arg
NM_001278409.2:c.13G>C	NP_001265338.1:p.Gly5Arg
NM_145869.2:c.112G>C	NP_665876.1:p.Gly38Arg
NM_001278408.2:c.112G>C	NP_001265337.1:p.Gly38Arg