Canonical Allele Identifier: CA358037209
Gene: ANXA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686296T>C , CM000666.2:g.121686296T>C GRCh38
NC_000004.11:g.122607451T>C , CM000666.1:g.122607451T>C GRCh37
NC_000004.10:g.122826901T>C NCBI36
NG_032042.1:g.15697A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.86A>G MANE Select ENSP00000296511.5:p.Lys29Arg
ENST00000296511.9:c.86A>G ENSP00000296511.5:p.Lys29Arg
ENST00000501272.6:c.10-2819A>G ENSP00000424106.1:n.10-2819A>G
ENST00000506395.5:c.86A>G ENSP00000421421.1:p.Lys29Arg
ENST00000509016.5:n.207A>G
ENST00000511552.5:n.472A>G
ENST00000513428.5:n.251A>G
ENST00000513523.1:n.254A>G
ENST00000513728.1:c.86A>G ENSP00000427135.1:p.Lys29Arg
ENST00000515017.5:c.86A>G ENSP00000424199.1:p.Lys29Arg
NM_001154.3:c.86A>G NP_001145.1:p.Lys29Arg
XM_017008141.2:c.86A>G XP_016863630.1:p.Lys29Arg
NM_001154.4:c.86A>G MANE Select NP_001145.1:p.Lys29Arg