Canonical Allele Identifier: CA1489955217
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121693486T= , CM000666.2:g.121693486T= GRCh38
NC_000004.11:g.122614641T= , CM000666.1:g.122614641T= GRCh37
NC_000004.10:g.122834091T= NCBI36
NG_032042.1:g.8507A=

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.9+3095A= MANE Select ENSP00000296511.5:n.9+3095A=
ENST00000296511.9:c.9+3095A= ENSP00000296511.5:n.9+3095A=
ENST00000501272.6:c.9+3095A= ENSP00000424106.1:n.9+3095A=
ENST00000506395.5:c.9+3095A= ENSP00000421421.1:n.9+3095A=
ENST00000509016.5:n.130+3377A=
ENST00000511552.5:n.395+3095A=
ENST00000513428.5:n.174+3095A=
ENST00000513523.1:n.177+3095A=
ENST00000513728.1:c.9+3095A= ENSP00000427135.1:n.9+3095A=
ENST00000515017.5:c.9+3095A= ENSP00000424199.1:n.9+3095A=
NM_001154.3:c.9+3095A= NP_001145.1:n.9+3095A=
XM_017008141.2:c.9+3095A= XP_016863630.1:n.9+3095A=
NM_001154.4:c.9+3095A= MANE Select NP_001145.1:n.9+3095A=