Canonical Allele Identifier: CA1489952018
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121685992C= , CM000666.2:g.121685992C= GRCh38
NC_000004.11:g.122607147C= , CM000666.1:g.122607147C= GRCh37
NC_000004.10:g.122826597C= NCBI36
NG_032042.1:g.16001G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+296G= MANE Select ENSP00000296511.5:n.94+296G=
ENST00000296511.9:c.94+296G= ENSP00000296511.5:n.94+296G=
ENST00000501272.6:c.10-2515G= ENSP00000424106.1:n.10-2515G=
ENST00000506395.5:c.94+296G= ENSP00000421421.1:n.94+296G=
ENST00000509016.5:n.215+296G=
ENST00000511552.5:n.480+296G=
ENST00000513428.5:n.259+296G=
ENST00000513523.1:n.262+296G=
ENST00000513728.1:c.94+296G= ENSP00000427135.1:n.94+296G=
ENST00000515017.5:c.94+296G= ENSP00000424199.1:n.94+296G=
NM_001154.3:c.94+296G= NP_001145.1:n.94+296G=
XM_017008141.2:c.94+296G= XP_016863630.1:n.94+296G=
NM_001154.4:c.94+296G= MANE Select NP_001145.1:n.94+296G=