Canonical Allele Identifier: CA358037517
Gene: ANXA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686365C>G , CM000666.2:g.121686365C>G GRCh38
NC_000004.11:g.122607520C>G , CM000666.1:g.122607520C>G GRCh37
NC_000004.10:g.122826970C>G NCBI36
NG_032042.1:g.15628G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.17G>C MANE Select ENSP00000296511.5:p.Arg6Thr
ENST00000296511.9:c.17G>C ENSP00000296511.5:p.Arg6Thr
ENST00000501272.6:c.10-2888G>C ENSP00000424106.1:n.10-2888G>C
ENST00000506395.5:c.17G>C ENSP00000421421.1:p.Arg6Thr
ENST00000509016.5:n.138G>C
ENST00000511552.5:n.403G>C
ENST00000513428.5:n.182G>C
ENST00000513523.1:n.185G>C
ENST00000513728.1:c.17G>C ENSP00000427135.1:p.Arg6Thr
ENST00000515017.5:c.17G>C ENSP00000424199.1:p.Arg6Thr
NM_001154.3:c.17G>C NP_001145.1:p.Arg6Thr
XM_017008141.2:c.17G>C XP_016863630.1:p.Arg6Thr
NM_001154.4:c.17G>C MANE Select NP_001145.1:p.Arg6Thr