Canonical Allele Identifier: CA2604058119
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs2110487313

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121685521del , CM000666.2:g.121685521del GRCh38
NC_000004.11:g.122606676del , CM000666.1:g.122606676del GRCh37
NC_000004.10:g.122826126del NCBI36
NG_032042.1:g.16472del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.95-750del MANE Select ENSP00000296511.5:n.95-750del
ENST00000296511.9:c.95-750del ENSP00000296511.5:n.95-750del
ENST00000501272.6:c.10-2044del ENSP00000424106.1:n.10-2044del
ENST00000506395.5:c.95-750del ENSP00000421421.1:n.95-750del
ENST00000509016.5:n.216-750del
ENST00000511552.5:n.481-750del
ENST00000513428.5:n.260-750del
ENST00000513523.1:n.262+767del
ENST00000513728.1:c.94+767del ENSP00000427135.1:n.94+767del
ENST00000515017.5:c.94+767del ENSP00000424199.1:n.94+767del
NM_001154.3:c.95-750del NP_001145.1:n.95-750del
XM_017008141.2:c.95-750del XP_016863630.1:n.95-750del
NM_001154.4:c.95-750del MANE Select NP_001145.1:n.95-750del