Canonical Allele Identifier: CA1489952110
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686132G= , CM000666.2:g.121686132G= GRCh38
NC_000004.11:g.122607287G= , CM000666.1:g.122607287G= GRCh37
NC_000004.10:g.122826737G= NCBI36
NG_032042.1:g.15861C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.94+156C= MANE Select ENSP00000296511.5:n.94+156C=
ENST00000296511.9:c.94+156C= ENSP00000296511.5:n.94+156C=
ENST00000501272.6:c.10-2655C= ENSP00000424106.1:n.10-2655C=
ENST00000506395.5:c.94+156C= ENSP00000421421.1:n.94+156C=
ENST00000509016.5:n.215+156C=
ENST00000511552.5:n.480+156C=
ENST00000513428.5:n.259+156C=
ENST00000513523.1:n.262+156C=
ENST00000513728.1:c.94+156C= ENSP00000427135.1:n.94+156C=
ENST00000515017.5:c.94+156C= ENSP00000424199.1:n.94+156C=
NM_001154.3:c.94+156C= NP_001145.1:n.94+156C=
XM_017008141.2:c.94+156C= XP_016863630.1:n.94+156C=
NM_001154.4:c.94+156C= MANE Select NP_001145.1:n.94+156C=