Canonical Allele Identifier: CA1489951791

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121685515C= , CM000666.2:g.121685515C=	GRCh38
NC_000004.11:g.122606670C= , CM000666.1:g.122606670C=	GRCh37
NC_000004.10:g.122826120C=	NCBI36
NG_032042.1:g.16478G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.95-744G= MANE Select	ENSP00000296511.5:n.95-744G=
ENST00000296511.9:c.95-744G=	ENSP00000296511.5:n.95-744G=
ENST00000501272.6:c.10-2038G=	ENSP00000424106.1:n.10-2038G=
ENST00000506395.5:c.95-744G=	ENSP00000421421.1:n.95-744G=
ENST00000509016.5:n.216-744G=
ENST00000511552.5:n.481-744G=
ENST00000513428.5:n.260-744G=
ENST00000513523.1:n.262+773G=
ENST00000513728.1:c.94+773G=	ENSP00000427135.1:n.94+773G=
ENST00000515017.5:c.94+773G=	ENSP00000424199.1:n.94+773G=
NM_001154.3:c.95-744G=	NP_001145.1:n.95-744G=
XM_017008141.2:c.95-744G=	XP_016863630.1:n.95-744G=
NM_001154.4:c.95-744G= MANE Select	NP_001145.1:n.95-744G=