Canonical Allele Identifier: CA1489951800

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121685530G= , CM000666.2:g.121685530G=	GRCh38
NC_000004.11:g.122606685G= , CM000666.1:g.122606685G=	GRCh37
NC_000004.10:g.122826135G=	NCBI36
NG_032042.1:g.16463C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.95-759C= MANE Select	ENSP00000296511.5:n.95-759C=
ENST00000296511.9:c.95-759C=	ENSP00000296511.5:n.95-759C=
ENST00000501272.6:c.10-2053C=	ENSP00000424106.1:n.10-2053C=
ENST00000506395.5:c.95-759C=	ENSP00000421421.1:n.95-759C=
ENST00000509016.5:n.216-759C=
ENST00000511552.5:n.481-759C=
ENST00000513428.5:n.260-759C=
ENST00000513523.1:n.262+758C=
ENST00000513728.1:c.94+758C=	ENSP00000427135.1:n.94+758C=
ENST00000515017.5:c.94+758C=	ENSP00000424199.1:n.94+758C=
NM_001154.3:c.95-759C=	NP_001145.1:n.95-759C=
XM_017008141.2:c.95-759C=	XP_016863630.1:n.95-759C=
NM_001154.4:c.95-759C= MANE Select	NP_001145.1:n.95-759C=