Canonical Allele Identifier: CA2671937174
Gene: ANXA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686167_121686169del , CM000666.2:g.121686167_121686169del GRCh38
NC_000004.11:g.122607322_122607324del , CM000666.1:g.122607322_122607324del GRCh37
NC_000004.10:g.122826772_122826774del NCBI36
NG_032042.1:g.15825_15827del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.94+120_94+122del MANE Select ENSP00000296511.5:n.94+120_94+122del
ENST00000296511.9:c.94+120_94+122del ENSP00000296511.5:n.94+120_94+122del
ENST00000501272.6:c.10-2691_10-2689del ENSP00000424106.1:n.10-2691_10-2689del
ENST00000506395.5:c.94+120_94+122del ENSP00000421421.1:n.94+120_94+122del
ENST00000509016.5:n.215+120_215+122del
ENST00000511552.5:n.480+120_480+122del
ENST00000513428.5:n.259+120_259+122del
ENST00000513523.1:n.262+120_262+122del
ENST00000513728.1:c.94+120_94+122del ENSP00000427135.1:n.94+120_94+122del
ENST00000515017.5:c.94+120_94+122del ENSP00000424199.1:n.94+120_94+122del
NM_001154.3:c.94+120_94+122del NP_001145.1:n.94+120_94+122del
XM_017008141.2:c.94+120_94+122del XP_016863630.1:n.94+120_94+122del
NM_001154.4:c.94+120_94+122del MANE Select NP_001145.1:n.94+120_94+122del