Canonical Allele Identifier: CA1067436763
Gene: ANXA5 HGNC NCBI

Linked Data

dbSNP Id: rs1725094375

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121696878C>G , CM000666.2:g.121696878C>G GRCh38
NC_000004.11:g.122618033C>G , CM000666.1:g.122618033C>G GRCh37
NC_000004.10:g.122837483C>G NCBI36
NG_032042.1:g.5115G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.-51G>C MANE Select ENSP00000296511.5:n.-51G>C
ENST00000296511.9:c.-51G>C ENSP00000296511.5:n.-51G>C
ENST00000501272.6:c.-51G>C ENSP00000424106.1:n.-51G>C
ENST00000506395.5:c.-51G>C ENSP00000421421.1:n.-51G>C
ENST00000509016.5:n.115G>C
ENST00000511552.5:n.98G>C
ENST00000513428.5:n.115G>C
ENST00000513523.1:n.118G>C
ENST00000513728.1:c.-51G>C ENSP00000427135.1:n.-51G>C
ENST00000515017.5:c.-51G>C ENSP00000424199.1:n.-51G>C
NM_001154.3:c.-51G>C NP_001145.1:n.-51G>C
XM_017008141.2:c.-51G>C XP_016863630.1:n.-51G>C
NM_001154.4:c.-51G>C MANE Select NP_001145.1:n.-51G>C