Canonical Allele Identifier: CA1067430927
Gene: ANXA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686045_121686046del , CM000666.2:g.121686045_121686046del GRCh38
NC_000004.11:g.122607200_122607201del , CM000666.1:g.122607200_122607201del GRCh37
NC_000004.10:g.122826650_122826651del NCBI36
NG_032042.1:g.15947_15948del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.94+242_94+243del MANE Select ENSP00000296511.5:n.94+242_94+243del
ENST00000296511.9:c.94+242_94+243del ENSP00000296511.5:n.94+242_94+243del
ENST00000501272.6:c.10-2569_10-2568del ENSP00000424106.1:n.10-2569_10-2568del
ENST00000506395.5:c.94+242_94+243del ENSP00000421421.1:n.94+242_94+243del
ENST00000509016.5:n.215+242_215+243del
ENST00000511552.5:n.480+242_480+243del
ENST00000513428.5:n.259+242_259+243del
ENST00000513523.1:n.262+242_262+243del
ENST00000513728.1:c.94+242_94+243del ENSP00000427135.1:n.94+242_94+243del
ENST00000515017.5:c.94+242_94+243del ENSP00000424199.1:n.94+242_94+243del
NM_001154.3:c.94+242_94+243del NP_001145.1:n.94+242_94+243del
XM_017008141.2:c.94+242_94+243del XP_016863630.1:n.94+242_94+243del
NM_001154.4:c.94+242_94+243del MANE Select NP_001145.1:n.94+242_94+243del