Canonical Allele Identifier: CA1489952188

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686331C= , CM000666.2:g.121686331C=	GRCh38
NC_000004.11:g.122607486C= , CM000666.1:g.122607486C=	GRCh37
NC_000004.10:g.122826936C=	NCBI36
NG_032042.1:g.15662G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.51G= MANE Select	ENSP00000296511.5:p.Glu17=
ENST00000296511.9:c.51G=	ENSP00000296511.5:p.Glu17=
ENST00000501272.6:c.10-2854G=	ENSP00000424106.1:n.10-2854G=
ENST00000506395.5:c.51G=	ENSP00000421421.1:p.Glu17=
ENST00000509016.5:n.172G=
ENST00000511552.5:n.437G=
ENST00000513428.5:n.216G=
ENST00000513523.1:n.219G=
ENST00000513728.1:c.51G=	ENSP00000427135.1:p.Glu17=
ENST00000515017.5:c.51G=	ENSP00000424199.1:p.Glu17=
NM_001154.3:c.51G=	NP_001145.1:p.Glu17=
XM_017008141.2:c.51G=	XP_016863630.1:p.Glu17=
NM_001154.4:c.51G= MANE Select	NP_001145.1:p.Glu17=