Canonical Allele Identifier: CA104723142
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs60663589

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686044dup , CM000666.2:g.121686044dup GRCh38
NC_000004.11:g.122607199dup , CM000666.1:g.122607199dup GRCh37
NC_000004.10:g.122826649dup NCBI36
NG_032042.1:g.15963dup

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+258dup MANE Select ENSP00000296511.5:n.94+258dup
ENST00000296511.9:c.94+258dup ENSP00000296511.5:n.94+258dup
ENST00000501272.6:c.10-2553dup ENSP00000424106.1:n.10-2553dup
ENST00000506395.5:c.94+258dup ENSP00000421421.1:n.94+258dup
ENST00000509016.5:n.215+258dup
ENST00000511552.5:n.480+258dup
ENST00000513428.5:n.259+258dup
ENST00000513523.1:n.262+258dup
ENST00000513728.1:c.94+258dup ENSP00000427135.1:n.94+258dup
ENST00000515017.5:c.94+258dup ENSP00000424199.1:n.94+258dup
NM_001154.3:c.94+258dup NP_001145.1:n.94+258dup
XM_017008141.2:c.94+258dup XP_016863630.1:n.94+258dup
NM_001154.4:c.94+258dup MANE Select NP_001145.1:n.94+258dup