Canonical Allele Identifier: CA1489951964
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1724879102
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121685884_121685905del , CM000666.2:g.121685884_121685905del GRCh38
NC_000004.11:g.122607039_122607060del , CM000666.1:g.122607039_122607060del GRCh37
NC_000004.10:g.122826489_122826510del NCBI36
NG_032042.1:g.16089_16110del

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+384_94+405del MANE Select ENSP00000296511.5:n.94+384_94+405del
ENST00000296511.9:c.94+384_94+405del ENSP00000296511.5:n.94+384_94+405del
ENST00000501272.6:c.10-2427_10-2406del ENSP00000424106.1:n.10-2427_10-2406del
ENST00000506395.5:c.94+384_94+405del ENSP00000421421.1:n.94+384_94+405del
ENST00000509016.5:n.215+384_215+405del
ENST00000511552.5:n.480+384_480+405del
ENST00000513428.5:n.259+384_259+405del
ENST00000513523.1:n.262+384_262+405del
ENST00000513728.1:c.94+384_94+405del ENSP00000427135.1:n.94+384_94+405del
ENST00000515017.5:c.94+384_94+405del ENSP00000424199.1:n.94+384_94+405del
NM_001154.3:c.94+384_94+405del NP_001145.1:n.94+384_94+405del
XM_017008141.2:c.94+384_94+405del XP_016863630.1:n.94+384_94+405del
NM_001154.4:c.94+384_94+405del MANE Select NP_001145.1:n.94+384_94+405del
Search 100 bp 5'
Search 100 bp 3'