Canonical Allele Identifier: CA1489952181

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686316T= , CM000666.2:g.121686316T=	GRCh38
NC_000004.11:g.122607471T= , CM000666.1:g.122607471T=	GRCh37
NC_000004.10:g.122826921T=	NCBI36
NG_032042.1:g.15677A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.66A= MANE Select	ENSP00000296511.5:p.Glu22=
ENST00000296511.9:c.66A=	ENSP00000296511.5:p.Glu22=
ENST00000501272.6:c.10-2839A=	ENSP00000424106.1:n.10-2839A=
ENST00000506395.5:c.66A=	ENSP00000421421.1:p.Glu22=
ENST00000509016.5:n.187A=
ENST00000511552.5:n.452A=
ENST00000513428.5:n.231A=
ENST00000513523.1:n.234A=
ENST00000513728.1:c.66A=	ENSP00000427135.1:p.Glu22=
ENST00000515017.5:c.66A=	ENSP00000424199.1:p.Glu22=
NM_001154.3:c.66A=	NP_001145.1:p.Glu22=
XM_017008141.2:c.66A=	XP_016863630.1:p.Glu22=
NM_001154.4:c.66A= MANE Select	NP_001145.1:p.Glu22=