Canonical Allele Identifier: CA2671938003
Gene: ANXA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121696887del , CM000666.2:g.121696887del GRCh38
NC_000004.11:g.122618042del , CM000666.1:g.122618042del GRCh37
NC_000004.10:g.122837492del NCBI36
NG_032042.1:g.5109del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.-57del MANE Select ENSP00000296511.5:n.-57del
ENST00000296511.9:c.-57del ENSP00000296511.5:n.-57del
ENST00000501272.6:c.-57del ENSP00000424106.1:n.-57del
ENST00000506395.5:c.-57del ENSP00000421421.1:n.-57del
ENST00000509016.5:n.109del
ENST00000511552.5:n.92del
ENST00000513428.5:n.109del
ENST00000513523.1:n.112del
ENST00000513728.1:c.-57del ENSP00000427135.1:n.-57del
ENST00000515017.5:c.-57del ENSP00000424199.1:n.-57del
NM_001154.3:c.-57del NP_001145.1:n.-57del
XM_017008141.2:c.-57del XP_016863630.1:n.-57del
NM_001154.4:c.-57del MANE Select NP_001145.1:n.-57del