Canonical Allele Identifier: CA2763335248
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686085_121686086del , CM000666.2:g.121686085_121686086del GRCh38
NC_000004.11:g.122607240_122607241del , CM000666.1:g.122607240_122607241del GRCh37
NC_000004.10:g.122826690_122826691del NCBI36
NG_032042.1:g.15907_15908del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.94+202_94+203del MANE Select ENSP00000296511.5:n.94+202_94+203del
ENST00000296511.9:c.94+202_94+203del ENSP00000296511.5:n.94+202_94+203del
ENST00000501272.6:c.10-2609_10-2608del ENSP00000424106.1:n.10-2609_10-2608del
ENST00000506395.5:c.94+202_94+203del ENSP00000421421.1:n.94+202_94+203del
ENST00000509016.5:n.215+202_215+203del
ENST00000511552.5:n.480+202_480+203del
ENST00000513428.5:n.259+202_259+203del
ENST00000513523.1:n.262+202_262+203del
ENST00000513728.1:c.94+202_94+203del ENSP00000427135.1:n.94+202_94+203del
ENST00000515017.5:c.94+202_94+203del ENSP00000424199.1:n.94+202_94+203del
NM_001154.3:c.94+202_94+203del NP_001145.1:n.94+202_94+203del
XM_017008141.2:c.94+202_94+203del XP_016863630.1:n.94+202_94+203del
NM_001154.4:c.94+202_94+203del MANE Select NP_001145.1:n.94+202_94+203del