Canonical Allele Identifier: CA358037523
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1724890333

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686366T>A , CM000666.2:g.121686366T>A GRCh38
NC_000004.11:g.122607521T>A , CM000666.1:g.122607521T>A GRCh37
NC_000004.10:g.122826971T>A NCBI36
NG_032042.1:g.15627A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.16A>T MANE Select ENSP00000296511.5:p.Arg6Ter
ENST00000296511.9:c.16A>T ENSP00000296511.5:p.Arg6Ter
ENST00000501272.6:c.10-2889A>T ENSP00000424106.1:n.10-2889A>T
ENST00000506395.5:c.16A>T ENSP00000421421.1:p.Arg6Ter
ENST00000509016.5:n.137A>T
ENST00000511552.5:n.402A>T
ENST00000513428.5:n.181A>T
ENST00000513523.1:n.184A>T
ENST00000513728.1:c.16A>T ENSP00000427135.1:p.Arg6Ter
ENST00000515017.5:c.16A>T ENSP00000424199.1:p.Arg6Ter
NM_001154.3:c.16A>T NP_001145.1:p.Arg6Ter
XM_017008141.2:c.16A>T XP_016863630.1:p.Arg6Ter
NM_001154.4:c.16A>T MANE Select NP_001145.1:p.Arg6Ter