Canonical Allele Identifier: CA104718517

Gene: ANXA5

Linked Data

• dbSNP Id: rs187370278
• gnomAD v3: 4-121679401-A-T
• gnomAD v4: 4-121679401-A-T
• MyVariant Identifiers: chr4:g.122600556A>T (hg19) ; chr4:g.121679401A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121679401A>T , CM000666.2:g.121679401A>T	GRCh38
NC_000004.11:g.122600556A>T , CM000666.1:g.122600556A>T	GRCh37
NC_000004.10:g.122820006A>T	NCBI36
NG_032042.1:g.22592T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.395-907T>A MANE Select	ENSP00000296511.5:n.395-907T>A
ENST00000296511.9:c.395-907T>A	ENSP00000296511.5:n.395-907T>A
ENST00000501272.6:c.215-907T>A	ENSP00000424106.1:n.215-907T>A
ENST00000506395.5:c.395-907T>A	ENSP00000421421.1:n.395-907T>A
ENST00000509016.5:n.516-907T>A
ENST00000511552.5:n.781-907T>A
ENST00000515017.5:c.95-907T>A	ENSP00000424199.1:n.95-907T>A
NM_001154.3:c.395-907T>A	NP_001145.1:n.395-907T>A
NM_001154.4:c.395-907T>A MANE Select	NP_001145.1:n.395-907T>A