Canonical Allele Identifier: CA1489949202
Gene: ANXA5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121679329C= , CM000666.2:g.121679329C= GRCh38
NC_000004.11:g.122600484C= , CM000666.1:g.122600484C= GRCh37
NC_000004.10:g.122819934C= NCBI36
NG_032042.1:g.22664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.395-835G= MANE Select ENSP00000296511.5:n.395-835G=
ENST00000296511.9:c.395-835G= ENSP00000296511.5:n.395-835G=
ENST00000501272.6:c.215-835G= ENSP00000424106.1:n.215-835G=
ENST00000506395.5:c.395-835G= ENSP00000421421.1:n.395-835G=
ENST00000509016.5:n.516-835G=
ENST00000511552.5:n.781-835G=
ENST00000515017.5:c.95-835G= ENSP00000424199.1:n.95-835G=
NM_001154.3:c.395-835G= NP_001145.1:n.395-835G=
NM_001154.4:c.395-835G= MANE Select NP_001145.1:n.395-835G=
Search 100 bp 5'
Search 100 bp 3'