Canonical Allele Identifier: CA1489956928

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696905G= , CM000666.2:g.121696905G=	GRCh38
NC_000004.11:g.122618060G= , CM000666.1:g.122618060G=	GRCh37
NC_000004.10:g.122837510G=	NCBI36
NG_032042.1:g.5088C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.-78C= MANE Select	ENSP00000296511.5:n.-78C=
ENST00000296511.9:c.-78C=	ENSP00000296511.5:n.-78C=
ENST00000501272.6:c.-78C=	ENSP00000424106.1:n.-78C=
ENST00000506395.5:c.-78C=	ENSP00000421421.1:n.-78C=
ENST00000509016.5:n.88C=
ENST00000511552.5:n.71C=
ENST00000513428.5:n.88C=
ENST00000513523.1:n.91C=
ENST00000513728.1:c.-78C=	ENSP00000427135.1:n.-78C=
ENST00000515017.5:c.-78C=	ENSP00000424199.1:n.-78C=
NM_001154.3:c.-78C=	NP_001145.1:n.-78C=
XM_017008141.2:c.-78C=	XP_016863630.1:n.-78C=
NM_001154.4:c.-78C= MANE Select	NP_001145.1:n.-78C=