Canonical Allele Identifier: CA1489951804

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121685541_121685542delinsCT , CM000666.2:g.121685541_121685542delinsCT	GRCh38
NC_000004.11:g.122606696_122606697delinsCT , CM000666.1:g.122606696_122606697delinsCT	GRCh37
NC_000004.10:g.122826146_122826147delinsCT	NCBI36
NG_032042.1:g.16451_16452delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+746_94+747delinsAG MANE Select	ENSP00000296511.5:n.94+746_94+747delinsAG
ENST00000296511.9:c.94+746_94+747delinsAG	ENSP00000296511.5:n.94+746_94+747delinsAG
ENST00000501272.6:c.10-2065_10-2064delinsAG	ENSP00000424106.1:n.10-2065_10-2064delinsAG
ENST00000506395.5:c.94+746_94+747delinsAG	ENSP00000421421.1:n.94+746_94+747delinsAG
ENST00000509016.5:n.215+746_215+747delinsAG
ENST00000511552.5:n.480+746_480+747delinsAG
ENST00000513428.5:n.259+746_259+747delinsAG
ENST00000513523.1:n.262+746_262+747delinsAG
ENST00000513728.1:c.94+746_94+747delinsAG	ENSP00000427135.1:n.94+746_94+747delinsAG
ENST00000515017.5:c.94+746_94+747delinsAG	ENSP00000424199.1:n.94+746_94+747delinsAG
NM_001154.3:c.94+746_94+747delinsAG	NP_001145.1:n.94+746_94+747delinsAG
XM_017008141.2:c.94+746_94+747delinsAG	XP_016863630.1:n.94+746_94+747delinsAG
NM_001154.4:c.94+746_94+747delinsAG MANE Select	NP_001145.1:n.94+746_94+747delinsAG