Canonical Allele Identifier: CA3062973
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121683371G>A , CM000666.2:g.121683371G>A GRCh38
NC_000004.11:g.122604526G>A , CM000666.1:g.122604526G>A GRCh37
NC_000004.10:g.122823976G>A NCBI36
NG_032042.1:g.18622C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001154.4:c.296C>T MANE Select NP_001145.1:p.Ala99Val
ENST00000296511.10:c.296C>T MANE Select ENSP00000296511.5:p.Ala99Val
NM_001154.3:c.296C>T NP_001145.1:p.Ala99Val
ENST00000296511.9:c.296C>T ENSP00000296511.5:p.Ala99Val
ENST00000501272.6:c.116C>T ENSP00000424106.1:p.Ala39Val
ENST00000506395.5:c.296C>T ENSP00000421421.1:p.Ala99Val
ENST00000509016.5:n.417C>T
ENST00000511552.5:n.682C>T
ENST00000513428.5:n.461C>T
ENST00000513523.1:n.369C>T
ENST00000513728.1:c.*93C>T ENSP00000427135.1:n.*93C>T
ENST00000515017.5:c.94+2917C>T ENSP00000424199.1:n.94+2917C>T
XM_017008141.2:c.296C>T XP_016863630.1:p.Ala99Val