Canonical Allele Identifier: CA2706872596

Gene: ANXA5

Linked Data

• dbSNP Id: rs71599155

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686030_121686031insGTT , CM000666.2:g.121686030_121686031insGTT	GRCh38
NC_000004.11:g.122607185_122607186insGTT , CM000666.1:g.122607185_122607186insGTT	GRCh37
NC_000004.10:g.122826635_122826636insGTT	NCBI36
NG_032042.1:g.15963_15964insACA

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.94+258_94+259insACA MANE Select	ENSP00000296511.5:n.94+258_94+259insACA
ENST00000296511.9:c.94+258_94+259insACA	ENSP00000296511.5:n.94+258_94+259insACA
ENST00000501272.6:c.10-2553_10-2552insACA	ENSP00000424106.1:n.10-2553_10-2552insACA...
ENST00000506395.5:c.94+258_94+259insACA	ENSP00000421421.1:n.94+258_94+259insACA
ENST00000509016.5:n.215+258_215+259insACA
ENST00000511552.5:n.480+258_480+259insACA
ENST00000513428.5:n.259+258_259+259insACA
ENST00000513523.1:n.262+258_262+259insACA
ENST00000513728.1:c.94+258_94+259insACA	ENSP00000427135.1:n.94+258_94+259insACA
ENST00000515017.5:c.94+258_94+259insACA	ENSP00000424199.1:n.94+258_94+259insACA
NM_001154.3:c.94+258_94+259insACA	NP_001145.1:n.94+258_94+259insACA
XM_017008141.2:c.94+258_94+259insACA	XP_016863630.1:n.94+258_94+259insACA
NM_001154.4:c.94+258_94+259insACA MANE Select	NP_001145.1:n.94+258_94+259insACA