Canonical Allele Identifier: CA1489955282
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1725025394

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121693679T>C , CM000666.2:g.121693679T>C GRCh38
NC_000004.11:g.122614834T>C , CM000666.1:g.122614834T>C GRCh37
NC_000004.10:g.122834284T>C NCBI36
NG_032042.1:g.8314A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.9+2902A>G MANE Select ENSP00000296511.5:n.9+2902A>G
ENST00000296511.9:c.9+2902A>G ENSP00000296511.5:n.9+2902A>G
ENST00000501272.6:c.9+2902A>G ENSP00000424106.1:n.9+2902A>G
ENST00000506395.5:c.9+2902A>G ENSP00000421421.1:n.9+2902A>G
ENST00000509016.5:n.130+3184A>G
ENST00000511552.5:n.395+2902A>G
ENST00000513428.5:n.174+2902A>G
ENST00000513523.1:n.177+2902A>G
ENST00000513728.1:c.9+2902A>G ENSP00000427135.1:n.9+2902A>G
ENST00000515017.5:c.9+2902A>G ENSP00000424199.1:n.9+2902A>G
NM_001154.3:c.9+2902A>G NP_001145.1:n.9+2902A>G
XM_017008141.2:c.9+2902A>G XP_016863630.1:n.9+2902A>G
NM_001154.4:c.9+2902A>G MANE Select NP_001145.1:n.9+2902A>G