Canonical Allele Identifier: CA1489955334

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121693818_121693820delinsCAG , CM000666.2:g.121693818_121693820delinsCAG	GRCh38
NC_000004.11:g.122614973_122614975delinsCAG , CM000666.1:g.122614973_122614975delinsCAG	GRCh37
NC_000004.10:g.122834423_122834425delinsCAG	NCBI36
NG_032042.1:g.8173_8175delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.9+2761_9+2763delinsCTG MANE Select	ENSP00000296511.5:n.9+2761_9+2763delinsCTG
ENST00000296511.9:c.9+2761_9+2763delinsCTG	ENSP00000296511.5:n.9+2761_9+2763delinsCTG
ENST00000501272.6:c.9+2761_9+2763delinsCTG	ENSP00000424106.1:n.9+2761_9+2763delinsCTG
ENST00000506395.5:c.9+2761_9+2763delinsCTG	ENSP00000421421.1:n.9+2761_9+2763delinsCTG
ENST00000509016.5:n.130+3043_130+3045delinsCTG
ENST00000511552.5:n.395+2761_395+2763delinsCTG
ENST00000513428.5:n.174+2761_174+2763delinsCTG
ENST00000513523.1:n.177+2761_177+2763delinsCTG
ENST00000513728.1:c.9+2761_9+2763delinsCTG	ENSP00000427135.1:n.9+2761_9+2763delinsCTG
ENST00000515017.5:c.9+2761_9+2763delinsCTG	ENSP00000424199.1:n.9+2761_9+2763delinsCTG
NM_001154.3:c.9+2761_9+2763delinsCTG	NP_001145.1:n.9+2761_9+2763delinsCTG
XM_017008141.2:c.9+2761_9+2763delinsCTG	XP_016863630.1:n.9+2761_9+2763delinsCTG
NM_001154.4:c.9+2761_9+2763delinsCTG MANE Select	NP_001145.1:n.9+2761_9+2763delinsCTG