Canonical Allele Identifier: CA1489955208
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1725022535
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121693461del , CM000666.2:g.121693461del GRCh38
NC_000004.11:g.122614616del , CM000666.1:g.122614616del GRCh37
NC_000004.10:g.122834066del NCBI36
NG_032042.1:g.8535del

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.9+3123del MANE Select ENSP00000296511.5:n.9+3123del
ENST00000296511.9:c.9+3123del ENSP00000296511.5:n.9+3123del
ENST00000501272.6:c.9+3123del ENSP00000424106.1:n.9+3123del
ENST00000506395.5:c.9+3123del ENSP00000421421.1:n.9+3123del
ENST00000509016.5:n.130+3405del
ENST00000511552.5:n.395+3123del
ENST00000513428.5:n.174+3123del
ENST00000513523.1:n.177+3123del
ENST00000513728.1:c.9+3123del ENSP00000427135.1:n.9+3123del
ENST00000515017.5:c.9+3123del ENSP00000424199.1:n.9+3123del
NM_001154.3:c.9+3123del NP_001145.1:n.9+3123del
XM_017008141.2:c.9+3123del XP_016863630.1:n.9+3123del
NM_001154.4:c.9+3123del MANE Select NP_001145.1:n.9+3123del
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Search 100 bp 3'