Canonical Allele Identifier: CA1489956909

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696876C= , CM000666.2:g.121696876C=	GRCh38
NC_000004.11:g.122618031C= , CM000666.1:g.122618031C=	GRCh37
NC_000004.10:g.122837481C=	NCBI36
NG_032042.1:g.5117G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.-49G= MANE Select	ENSP00000296511.5:n.-49G=
ENST00000296511.9:c.-49G=	ENSP00000296511.5:n.-49G=
ENST00000501272.6:c.-49G=	ENSP00000424106.1:n.-49G=
ENST00000506395.5:c.-49G=	ENSP00000421421.1:n.-49G=
ENST00000509016.5:n.117G=
ENST00000511552.5:n.100G=
ENST00000513428.5:n.117G=
ENST00000513523.1:n.120G=
ENST00000513728.1:c.-49G=	ENSP00000427135.1:n.-49G=
ENST00000515017.5:c.-49G=	ENSP00000424199.1:n.-49G=
NM_001154.3:c.-49G=	NP_001145.1:n.-49G=
XM_017008141.2:c.-49G=	XP_016863630.1:n.-49G=
NM_001154.4:c.-49G= MANE Select	NP_001145.1:n.-49G=