Canonical Allele Identifier: CA2604058126
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs2110487585

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121685918_121685919dup , CM000666.2:g.121685918_121685919dup GRCh38
NC_000004.11:g.122607073_122607074dup , CM000666.1:g.122607073_122607074dup GRCh37
NC_000004.10:g.122826523_122826524dup NCBI36
NG_032042.1:g.16076_16077dup

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+371_94+372dup MANE Select ENSP00000296511.5:n.94+371_94+372dup
ENST00000296511.9:c.94+371_94+372dup ENSP00000296511.5:n.94+371_94+372dup
ENST00000501272.6:c.10-2440_10-2439dup ENSP00000424106.1:n.10-2440_10-2439dup
ENST00000506395.5:c.94+371_94+372dup ENSP00000421421.1:n.94+371_94+372dup
ENST00000509016.5:n.215+371_215+372dup
ENST00000511552.5:n.480+371_480+372dup
ENST00000513428.5:n.259+371_259+372dup
ENST00000513523.1:n.262+371_262+372dup
ENST00000513728.1:c.94+371_94+372dup ENSP00000427135.1:n.94+371_94+372dup
ENST00000515017.5:c.94+371_94+372dup ENSP00000424199.1:n.94+371_94+372dup
NM_001154.3:c.94+371_94+372dup NP_001145.1:n.94+371_94+372dup
XM_017008141.2:c.94+371_94+372dup XP_016863630.1:n.94+371_94+372dup
NM_001154.4:c.94+371_94+372dup MANE Select NP_001145.1:n.94+371_94+372dup