Canonical Allele Identifier: CA1067430968
Gene: ANXA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686049_121686060del , CM000666.2:g.121686049_121686060del GRCh38
NC_000004.11:g.122607204_122607215del , CM000666.1:g.122607204_122607215del GRCh37
NC_000004.10:g.122826654_122826665del NCBI36
NG_032042.1:g.15933_15944del

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+228_94+239del MANE Select ENSP00000296511.5:n.94+228_94+239del
ENST00000296511.9:c.94+228_94+239del ENSP00000296511.5:n.94+228_94+239del
ENST00000501272.6:c.10-2583_10-2572del ENSP00000424106.1:n.10-2583_10-2572del
ENST00000506395.5:c.94+228_94+239del ENSP00000421421.1:n.94+228_94+239del
ENST00000509016.5:n.215+228_215+239del
ENST00000511552.5:n.480+228_480+239del
ENST00000513428.5:n.259+228_259+239del
ENST00000513523.1:n.262+228_262+239del
ENST00000513728.1:c.94+228_94+239del ENSP00000427135.1:n.94+228_94+239del
ENST00000515017.5:c.94+228_94+239del ENSP00000424199.1:n.94+228_94+239del
NM_001154.3:c.94+228_94+239del NP_001145.1:n.94+228_94+239del
XM_017008141.2:c.94+228_94+239del XP_016863630.1:n.94+228_94+239del
NM_001154.4:c.94+228_94+239del MANE Select NP_001145.1:n.94+228_94+239del