Canonical Allele Identifier: CA1489952088
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1724884520

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686094T>C , CM000666.2:g.121686094T>C GRCh38
NC_000004.11:g.122607249T>C , CM000666.1:g.122607249T>C GRCh37
NC_000004.10:g.122826699T>C NCBI36
NG_032042.1:g.15899A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.94+194A>G MANE Select ENSP00000296511.5:n.94+194A>G
ENST00000296511.9:c.94+194A>G ENSP00000296511.5:n.94+194A>G
ENST00000501272.6:c.10-2617A>G ENSP00000424106.1:n.10-2617A>G
ENST00000506395.5:c.94+194A>G ENSP00000421421.1:n.94+194A>G
ENST00000509016.5:n.215+194A>G
ENST00000511552.5:n.480+194A>G
ENST00000513428.5:n.259+194A>G
ENST00000513523.1:n.262+194A>G
ENST00000513728.1:c.94+194A>G ENSP00000427135.1:n.94+194A>G
ENST00000515017.5:c.94+194A>G ENSP00000424199.1:n.94+194A>G
NM_001154.3:c.94+194A>G NP_001145.1:n.94+194A>G
XM_017008141.2:c.94+194A>G XP_016863630.1:n.94+194A>G
NM_001154.4:c.94+194A>G MANE Select NP_001145.1:n.94+194A>G