Canonical Allele Identifier: CA2763335518
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121679331G>C , CM000666.2:g.121679331G>C GRCh38
NC_000004.11:g.122600486G>C , CM000666.1:g.122600486G>C GRCh37
NC_000004.10:g.122819936G>C NCBI36
NG_032042.1:g.22662C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.395-837C>G MANE Select ENSP00000296511.5:n.395-837C>G
ENST00000296511.9:c.395-837C>G ENSP00000296511.5:n.395-837C>G
ENST00000501272.6:c.215-837C>G ENSP00000424106.1:n.215-837C>G
ENST00000506395.5:c.395-837C>G ENSP00000421421.1:n.395-837C>G
ENST00000509016.5:n.516-837C>G
ENST00000511552.5:n.781-837C>G
ENST00000515017.5:c.95-837C>G ENSP00000424199.1:n.95-837C>G
NM_001154.3:c.395-837C>G NP_001145.1:n.395-837C>G
NM_001154.4:c.395-837C>G MANE Select NP_001145.1:n.395-837C>G