Canonical Allele Identifier: CA1489952103
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1724885268

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686126dup , CM000666.2:g.121686126dup GRCh38
NC_000004.11:g.122607281dup , CM000666.1:g.122607281dup GRCh37
NC_000004.10:g.122826731dup NCBI36
NG_032042.1:g.15870dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.94+165dup MANE Select ENSP00000296511.5:n.94+165dup
ENST00000296511.9:c.94+165dup ENSP00000296511.5:n.94+165dup
ENST00000501272.6:c.10-2646dup ENSP00000424106.1:n.10-2646dup
ENST00000506395.5:c.94+165dup ENSP00000421421.1:n.94+165dup
ENST00000509016.5:n.215+165dup
ENST00000511552.5:n.480+165dup
ENST00000513428.5:n.259+165dup
ENST00000513523.1:n.262+165dup
ENST00000513728.1:c.94+165dup ENSP00000427135.1:n.94+165dup
ENST00000515017.5:c.94+165dup ENSP00000424199.1:n.94+165dup
NM_001154.3:c.94+165dup NP_001145.1:n.94+165dup
XM_017008141.2:c.94+165dup XP_016863630.1:n.94+165dup
NM_001154.4:c.94+165dup MANE Select NP_001145.1:n.94+165dup