Canonical Allele Identifier: CA1067431048
Gene: ANXA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686069_121686070del , CM000666.2:g.121686069_121686070del GRCh38
NC_000004.11:g.122607224_122607225del , CM000666.1:g.122607224_122607225del GRCh37
NC_000004.10:g.122826674_122826675del NCBI36
NG_032042.1:g.15923_15924del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.94+218_94+219del MANE Select ENSP00000296511.5:n.94+218_94+219del
ENST00000296511.9:c.94+218_94+219del ENSP00000296511.5:n.94+218_94+219del
ENST00000501272.6:c.10-2593_10-2592del ENSP00000424106.1:n.10-2593_10-2592del
ENST00000506395.5:c.94+218_94+219del ENSP00000421421.1:n.94+218_94+219del
ENST00000509016.5:n.215+218_215+219del
ENST00000511552.5:n.480+218_480+219del
ENST00000513428.5:n.259+218_259+219del
ENST00000513523.1:n.262+218_262+219del
ENST00000513728.1:c.94+218_94+219del ENSP00000427135.1:n.94+218_94+219del
ENST00000515017.5:c.94+218_94+219del ENSP00000424199.1:n.94+218_94+219del
NM_001154.3:c.94+218_94+219del NP_001145.1:n.94+218_94+219del
XM_017008141.2:c.94+218_94+219del XP_016863630.1:n.94+218_94+219del
NM_001154.4:c.94+218_94+219del MANE Select NP_001145.1:n.94+218_94+219del