Canonical Allele Identifier: CA1489949239

Gene: ANXA5

Linked Data

• dbSNP Id: rs1724753436

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121679418A>G , CM000666.2:g.121679418A>G	GRCh38
NC_000004.11:g.122600573A>G , CM000666.1:g.122600573A>G	GRCh37
NC_000004.10:g.122820023A>G	NCBI36
NG_032042.1:g.22575T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.395-924T>C MANE Select	ENSP00000296511.5:n.395-924T>C
ENST00000296511.9:c.395-924T>C	ENSP00000296511.5:n.395-924T>C
ENST00000501272.6:c.215-924T>C	ENSP00000424106.1:n.215-924T>C
ENST00000506395.5:c.395-924T>C	ENSP00000421421.1:n.395-924T>C
ENST00000509016.5:n.516-924T>C
ENST00000511552.5:n.781-924T>C
ENST00000515017.5:c.95-924T>C	ENSP00000424199.1:n.95-924T>C
NM_001154.3:c.395-924T>C	NP_001145.1:n.395-924T>C
NM_001154.4:c.395-924T>C MANE Select	NP_001145.1:n.395-924T>C