Canonical Allele Identifier: CA786352855

Gene: ANXA5

Linked Data

• dbSNP Id: rs71599155
• MyVariant Identifiers: chr4:g.122607184_122607185insTCT (hg19) ; chr4:g.121686029_121686030insTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686030_121686031insCTT , CM000666.2:g.121686030_121686031insCTT	GRCh38
NC_000004.11:g.122607185_122607186insCTT , CM000666.1:g.122607185_122607186insCTT	GRCh37
NC_000004.10:g.122826635_122826636insCTT	NCBI36
NG_032042.1:g.15963_15964insAGA

Transcript Alleles

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