Canonical Allele Identifier: CA917292096
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1578446496

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121685915_121685916insA , CM000666.2:g.121685915_121685916insA GRCh38
NC_000004.11:g.122607070_122607071insA , CM000666.1:g.122607070_122607071insA GRCh37
NC_000004.10:g.122826520_122826521insA NCBI36
NG_032042.1:g.16077_16078insT

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+372_94+373insT MANE Select ENSP00000296511.5:n.94+372_94+373insT
ENST00000296511.9:c.94+372_94+373insT ENSP00000296511.5:n.94+372_94+373insT
ENST00000501272.6:c.10-2439_10-2438insT ENSP00000424106.1:n.10-2439_10-2438insT
ENST00000506395.5:c.94+372_94+373insT ENSP00000421421.1:n.94+372_94+373insT
ENST00000509016.5:n.215+372_215+373insT
ENST00000511552.5:n.480+372_480+373insT
ENST00000513428.5:n.259+372_259+373insT
ENST00000513523.1:n.262+372_262+373insT
ENST00000513728.1:c.94+372_94+373insT ENSP00000427135.1:n.94+372_94+373insT
ENST00000515017.5:c.94+372_94+373insT ENSP00000424199.1:n.94+372_94+373insT
NM_001154.3:c.94+372_94+373insT NP_001145.1:n.94+372_94+373insT
XM_017008141.2:c.94+372_94+373insT XP_016863630.1:n.94+372_94+373insT
NM_001154.4:c.94+372_94+373insT MANE Select NP_001145.1:n.94+372_94+373insT