Canonical Allele Identifier: CA1489956967

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696961C= , CM000666.2:g.121696961C=	GRCh38
NC_000004.11:g.122618116C= , CM000666.1:g.122618116C=	GRCh37
NC_000004.10:g.122837566C=	NCBI36
NG_032042.1:g.5032G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.-134G= MANE Select	ENSP00000296511.5:n.-134G=
ENST00000296511.9:c.-134G=	ENSP00000296511.5:n.-134G=
ENST00000501272.6:c.-134G=	ENSP00000424106.1:n.-134G=
ENST00000506395.5:c.-134G=	ENSP00000421421.1:n.-134G=
ENST00000509016.5:n.32G=
ENST00000511552.5:n.15G=
ENST00000513428.5:n.32G=
ENST00000513523.1:n.35G=
ENST00000513728.1:c.-134G=	ENSP00000427135.1:n.-134G=
ENST00000515017.5:c.-134G=	ENSP00000424199.1:n.-134G=
NM_001154.3:c.-134G=	NP_001145.1:n.-134G=
XM_017008141.2:c.-134G=	XP_016863630.1:n.-134G=
NM_001154.4:c.-134G= MANE Select	NP_001145.1:n.-134G=