Canonical Allele Identifier: CA1489955279
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121693659_121693668delinsGCAAAGCAGC , CM000666.2:g.121693659_121693668delinsGCAAAGCAGC GRCh38
NC_000004.11:g.122614814_122614823delinsGCAAAGCAGC , CM000666.1:g.122614814_122614823delinsGCAAAGCAGC GRCh37
NC_000004.10:g.122834264_122834273delinsGCAAAGCAGC NCBI36
NG_032042.1:g.8325_8334delinsGCTGCTTTGC

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.9+2913_9+2922delinsGCTGCTTTGC MANE Select ENSP00000296511.5:n.9+2913_9+2922delinsGC...
ENST00000296511.9:c.9+2913_9+2922delinsGCTGCTTTGC ENSP00000296511.5:n.9+2913_9+2922delinsGC...
ENST00000501272.6:c.9+2913_9+2922delinsGCTGCTTTGC ENSP00000424106.1:n.9+2913_9+2922delinsGC...
ENST00000506395.5:c.9+2913_9+2922delinsGCTGCTTTGC ENSP00000421421.1:n.9+2913_9+2922delinsGC...
ENST00000509016.5:n.130+3195_130+3204delinsGCTGCTTTGC
ENST00000511552.5:n.395+2913_395+2922delinsGCTGCTTTGC
ENST00000513428.5:n.174+2913_174+2922delinsGCTGCTTTGC
ENST00000513523.1:n.177+2913_177+2922delinsGCTGCTTTGC
ENST00000513728.1:c.9+2913_9+2922delinsGCTGCTTTGC ENSP00000427135.1:n.9+2913_9+2922delinsGC...
ENST00000515017.5:c.9+2913_9+2922delinsGCTGCTTTGC ENSP00000424199.1:n.9+2913_9+2922delinsGC...
NM_001154.3:c.9+2913_9+2922delinsGCTGCTTTGC NP_001145.1:n.9+2913_9+2922delinsGCTGCTTT...
XM_017008141.2:c.9+2913_9+2922delinsGCTGCTTTGC XP_016863630.1:n.9+2913_9+2922delinsGCTGC...
NM_001154.4:c.9+2913_9+2922delinsGCTGCTTTGC MANE Select NP_001145.1:n.9+2913_9+2922delinsGCTGCTTT...