Canonical Allele Identifier: CA1489952035
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686020A= , CM000666.2:g.121686020A= GRCh38
NC_000004.11:g.122607175A= , CM000666.1:g.122607175A= GRCh37
NC_000004.10:g.122826625A= NCBI36
NG_032042.1:g.15973T=

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+268T= MANE Select ENSP00000296511.5:n.94+268T=
ENST00000296511.9:c.94+268T= ENSP00000296511.5:n.94+268T=
ENST00000501272.6:c.10-2543T= ENSP00000424106.1:n.10-2543T=
ENST00000506395.5:c.94+268T= ENSP00000421421.1:n.94+268T=
ENST00000509016.5:n.215+268T=
ENST00000511552.5:n.480+268T=
ENST00000513428.5:n.259+268T=
ENST00000513523.1:n.262+268T=
ENST00000513728.1:c.94+268T= ENSP00000427135.1:n.94+268T=
ENST00000515017.5:c.94+268T= ENSP00000424199.1:n.94+268T=
NM_001154.3:c.94+268T= NP_001145.1:n.94+268T=
XM_017008141.2:c.94+268T= XP_016863630.1:n.94+268T=
NM_001154.4:c.94+268T= MANE Select NP_001145.1:n.94+268T=