Canonical Allele Identifier: CA554174430
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1724883131

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686045_121686047del , CM000666.2:g.121686045_121686047del GRCh38
NC_000004.11:g.122607200_122607202del , CM000666.1:g.122607200_122607202del GRCh37
NC_000004.10:g.122826650_122826652del NCBI36
NG_032042.1:g.15946_15948del

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+241_94+243del MANE Select ENSP00000296511.5:n.94+241_94+243del
ENST00000296511.9:c.94+241_94+243del ENSP00000296511.5:n.94+241_94+243del
ENST00000501272.6:c.10-2570_10-2568del ENSP00000424106.1:n.10-2570_10-2568del
ENST00000506395.5:c.94+241_94+243del ENSP00000421421.1:n.94+241_94+243del
ENST00000509016.5:n.215+241_215+243del
ENST00000511552.5:n.480+241_480+243del
ENST00000513428.5:n.259+241_259+243del
ENST00000513523.1:n.262+241_262+243del
ENST00000513728.1:c.94+241_94+243del ENSP00000427135.1:n.94+241_94+243del
ENST00000515017.5:c.94+241_94+243del ENSP00000424199.1:n.94+241_94+243del
NM_001154.3:c.94+241_94+243del NP_001145.1:n.94+241_94+243del
XM_017008141.2:c.94+241_94+243del XP_016863630.1:n.94+241_94+243del
NM_001154.4:c.94+241_94+243del MANE Select NP_001145.1:n.94+241_94+243del