Canonical Allele Identifier: CA11872156
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs4833229

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121679509G>A , CM000666.2:g.121679509G>A GRCh38
NC_000004.11:g.122600664G>A , CM000666.1:g.122600664G>A GRCh37
NC_000004.10:g.122820114G>A NCBI36
NG_032042.1:g.22484C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.395-1015C>T MANE Select ENSP00000296511.5:p.=
ENST00000296511.9:c.395-1015C>T ENSP00000296511.5:p.=
ENST00000501272.6:c.215-1015C>T ENSP00000424106.1:p.=
ENST00000506395.5:c.395-1015C>T ENSP00000421421.1:p.=
ENST00000509016.5:n.516-1015C>T
ENST00000511552.5:n.781-1015C>T
ENST00000515017.5:c.95-1015C>T ENSP00000424199.1:p.=
NM_001154.3:c.395-1015C>T NP_001145.1:p.=
NM_001154.4:c.395-1015C>T MANE Select NP_001145.1:p.=