Canonical Allele Identifier: CA1489955072

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121693160_121693166delinsGGAAGCA , CM000666.2:g.121693160_121693166delinsGGAAGCA	GRCh38
NC_000004.11:g.122614315_122614321delinsGGAAGCA , CM000666.1:g.122614315_122614321delinsGGAAGCA	GRCh37
NC_000004.10:g.122833765_122833771delinsGGAAGCA	NCBI36
NG_032042.1:g.8827_8833delinsTGCTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.9+3415_9+3421delinsTGCTTCC MANE Select	ENSP00000296511.5:n.9+3415_9+3421delinsTGCTTCC
ENST00000296511.9:c.9+3415_9+3421delinsTGCTTCC	ENSP00000296511.5:n.9+3415_9+3421delinsTGCTTCC
ENST00000501272.6:c.9+3415_9+3421delinsTGCTTCC	ENSP00000424106.1:n.9+3415_9+3421delinsTGCTTCC
ENST00000506395.5:c.9+3415_9+3421delinsTGCTTCC	ENSP00000421421.1:n.9+3415_9+3421delinsTGCTTCC
ENST00000509016.5:n.130+3697_130+3703delinsTGCTTCC
ENST00000511552.5:n.395+3415_395+3421delinsTGCTTCC
ENST00000513428.5:n.174+3415_174+3421delinsTGCTTCC
ENST00000513523.1:n.177+3415_177+3421delinsTGCTTCC
ENST00000513728.1:c.9+3415_9+3421delinsTGCTTCC	ENSP00000427135.1:n.9+3415_9+3421delinsTGCTTCC
ENST00000515017.5:c.9+3415_9+3421delinsTGCTTCC	ENSP00000424199.1:n.9+3415_9+3421delinsTGCTTCC
NM_001154.3:c.9+3415_9+3421delinsTGCTTCC	NP_001145.1:n.9+3415_9+3421delinsTGCTTCC
XM_017008141.2:c.9+3415_9+3421delinsTGCTTCC	XP_016863630.1:n.9+3415_9+3421delinsTGCTTCC
NM_001154.4:c.9+3415_9+3421delinsTGCTTCC MANE Select	NP_001145.1:n.9+3415_9+3421delinsTGCTTCC