Canonical Allele Identifier: CA1489952236
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1724891730

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686419_121686420insTAGT , CM000666.2:g.121686419_121686420insTAGT GRCh38
NC_000004.11:g.122607574_122607575insTAGT , CM000666.1:g.122607574_122607575insTAGT GRCh37
NC_000004.10:g.122827024_122827025insTAGT NCBI36
NG_032042.1:g.15573_15574insACTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.10-48_10-47insACTA MANE Select ENSP00000296511.5:n.10-48_10-47insACTA
ENST00000296511.9:c.10-48_10-47insACTA ENSP00000296511.5:n.10-48_10-47insACTA
ENST00000501272.6:c.10-2943_10-2942insACTA ENSP00000424106.1:n.10-2943_10-2942insACTA
ENST00000506395.5:c.10-48_10-47insACTA ENSP00000421421.1:n.10-48_10-47insACTA
ENST00000509016.5:n.131-48_131-47insACTA
ENST00000511552.5:n.396-48_396-47insACTA
ENST00000513428.5:n.175-48_175-47insACTA
ENST00000513523.1:n.178-48_178-47insACTA
ENST00000513728.1:c.10-48_10-47insACTA ENSP00000427135.1:n.10-48_10-47insACTA
ENST00000515017.5:c.10-48_10-47insACTA ENSP00000424199.1:n.10-48_10-47insACTA
NM_001154.3:c.10-48_10-47insACTA NP_001145.1:n.10-48_10-47insACTA
XM_017008141.2:c.10-48_10-47insACTA XP_016863630.1:n.10-48_10-47insACTA
NM_001154.4:c.10-48_10-47insACTA MANE Select NP_001145.1:n.10-48_10-47insACTA