Canonical Allele Identifier: CA2763335229
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686031_121686032insGT , CM000666.2:g.121686031_121686032insGT GRCh38
NC_000004.11:g.122607186_122607187insGT , CM000666.1:g.122607186_122607187insGT GRCh37
NC_000004.10:g.122826636_122826637insGT NCBI36
NG_032042.1:g.15962_15963insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.94+257_94+258insCA MANE Select ENSP00000296511.5:n.94+257_94+258insCA
ENST00000296511.9:c.94+257_94+258insCA ENSP00000296511.5:n.94+257_94+258insCA
ENST00000501272.6:c.10-2554_10-2553insCA ENSP00000424106.1:n.10-2554_10-2553insCA
ENST00000506395.5:c.94+257_94+258insCA ENSP00000421421.1:n.94+257_94+258insCA
ENST00000509016.5:n.215+257_215+258insCA
ENST00000511552.5:n.480+257_480+258insCA
ENST00000513428.5:n.259+257_259+258insCA
ENST00000513523.1:n.262+257_262+258insCA
ENST00000513728.1:c.94+257_94+258insCA ENSP00000427135.1:n.94+257_94+258insCA
ENST00000515017.5:c.94+257_94+258insCA ENSP00000424199.1:n.94+257_94+258insCA
NM_001154.3:c.94+257_94+258insCA NP_001145.1:n.94+257_94+258insCA
XM_017008141.2:c.94+257_94+258insCA XP_016863630.1:n.94+257_94+258insCA
NM_001154.4:c.94+257_94+258insCA MANE Select NP_001145.1:n.94+257_94+258insCA