Canonical Allele Identifier: CA1489952270

Gene: ANXA5

Linked Data

• dbSNP Id: rs1724893030

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686493_121686494insCTG , CM000666.2:g.121686493_121686494insCTG	GRCh38
NC_000004.11:g.122607648_122607649insCTG , CM000666.1:g.122607648_122607649insCTG	GRCh37
NC_000004.10:g.122827098_122827099insCTG	NCBI36
NG_032042.1:g.15499_15500insCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-122_10-121insCAG MANE Select	ENSP00000296511.5:n.10-122_10-121insCAG
ENST00000296511.9:c.10-122_10-121insCAG	ENSP00000296511.5:n.10-122_10-121insCAG
ENST00000501272.6:c.10-3017_10-3016insCAG	ENSP00000424106.1:n.10-3017_10-3016insCAG
ENST00000506395.5:c.10-122_10-121insCAG	ENSP00000421421.1:n.10-122_10-121insCAG
ENST00000509016.5:n.131-122_131-121insCAG
ENST00000511552.5:n.396-122_396-121insCAG
ENST00000513428.5:n.175-122_175-121insCAG
ENST00000513523.1:n.178-122_178-121insCAG
ENST00000513728.1:c.10-122_10-121insCAG	ENSP00000427135.1:n.10-122_10-121insCAG
ENST00000515017.5:c.10-122_10-121insCAG	ENSP00000424199.1:n.10-122_10-121insCAG
NM_001154.3:c.10-122_10-121insCAG	NP_001145.1:n.10-122_10-121insCAG
XM_017008141.2:c.10-122_10-121insCAG	XP_016863630.1:n.10-122_10-121insCAG
NM_001154.4:c.10-122_10-121insCAG MANE Select	NP_001145.1:n.10-122_10-121insCAG