Canonical Allele Identifier: CA1489952032

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686017G= , CM000666.2:g.121686017G=	GRCh38
NC_000004.11:g.122607172G= , CM000666.1:g.122607172G=	GRCh37
NC_000004.10:g.122826622G=	NCBI36
NG_032042.1:g.15976C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+271C= MANE Select	ENSP00000296511.5:n.94+271C=
ENST00000296511.9:c.94+271C=	ENSP00000296511.5:n.94+271C=
ENST00000501272.6:c.10-2540C=	ENSP00000424106.1:n.10-2540C=
ENST00000506395.5:c.94+271C=	ENSP00000421421.1:n.94+271C=
ENST00000509016.5:n.215+271C=
ENST00000511552.5:n.480+271C=
ENST00000513428.5:n.259+271C=
ENST00000513523.1:n.262+271C=
ENST00000513728.1:c.94+271C=	ENSP00000427135.1:n.94+271C=
ENST00000515017.5:c.94+271C=	ENSP00000424199.1:n.94+271C=
NM_001154.3:c.94+271C=	NP_001145.1:n.94+271C=
XM_017008141.2:c.94+271C=	XP_016863630.1:n.94+271C=
NM_001154.4:c.94+271C= MANE Select	NP_001145.1:n.94+271C=