Canonical Allele Identifier: CA554175836
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1393592646

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121693331_121693332insGTTTACAT , CM000666.2:g.121693331_121693332insGTTTACAT GRCh38
NC_000004.11:g.122614486_122614487insGTTTACAT , CM000666.1:g.122614486_122614487insGTTTACAT GRCh37
NC_000004.10:g.122833936_122833937insGTTTACAT NCBI36
NG_032042.1:g.8663_8664insGTAAACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.9+3251_9+3252insGTAAACAT MANE Select ENSP00000296511.5:n.9+3251_9+3252insGTAAACAT
ENST00000296511.9:c.9+3251_9+3252insGTAAACAT ENSP00000296511.5:n.9+3251_9+3252insGTAAACAT
ENST00000501272.6:c.9+3251_9+3252insGTAAACAT ENSP00000424106.1:n.9+3251_9+3252insGTAAACAT
ENST00000506395.5:c.9+3251_9+3252insGTAAACAT ENSP00000421421.1:n.9+3251_9+3252insGTAAACAT
ENST00000509016.5:n.130+3533_130+3534insGTAAACAT
ENST00000511552.5:n.395+3251_395+3252insGTAAACAT
ENST00000513428.5:n.174+3251_174+3252insGTAAACAT
ENST00000513523.1:n.177+3251_177+3252insGTAAACAT
ENST00000513728.1:c.9+3251_9+3252insGTAAACAT ENSP00000427135.1:n.9+3251_9+3252insGTAAACAT
ENST00000515017.5:c.9+3251_9+3252insGTAAACAT ENSP00000424199.1:n.9+3251_9+3252insGTAAACAT
NM_001154.3:c.9+3251_9+3252insGTAAACAT NP_001145.1:n.9+3251_9+3252insGTAAACAT
XM_017008141.2:c.9+3251_9+3252insGTAAACAT XP_016863630.1:n.9+3251_9+3252insGTAAACAT
NM_001154.4:c.9+3251_9+3252insGTAAACAT MANE Select NP_001145.1:n.9+3251_9+3252insGTAAACAT