Canonical Allele Identifier: CA786352806
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1457466754

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121685975A>C , CM000666.2:g.121685975A>C GRCh38
NC_000004.11:g.122607130A>C , CM000666.1:g.122607130A>C GRCh37
NC_000004.10:g.122826580A>C NCBI36
NG_032042.1:g.16018T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+313T>G MANE Select ENSP00000296511.5:n.94+313T>G
ENST00000296511.9:c.94+313T>G ENSP00000296511.5:n.94+313T>G
ENST00000501272.6:c.10-2498T>G ENSP00000424106.1:n.10-2498T>G
ENST00000506395.5:c.94+313T>G ENSP00000421421.1:n.94+313T>G
ENST00000509016.5:n.215+313T>G
ENST00000511552.5:n.480+313T>G
ENST00000513428.5:n.259+313T>G
ENST00000513523.1:n.262+313T>G
ENST00000513728.1:c.94+313T>G ENSP00000427135.1:n.94+313T>G
ENST00000515017.5:c.94+313T>G ENSP00000424199.1:n.94+313T>G
NM_001154.3:c.94+313T>G NP_001145.1:n.94+313T>G
XM_017008141.2:c.94+313T>G XP_016863630.1:n.94+313T>G
NM_001154.4:c.94+313T>G MANE Select NP_001145.1:n.94+313T>G