Canonical Allele Identifier: CA1489955388

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121693955T= , CM000666.2:g.121693955T=	GRCh38
NC_000004.11:g.122615110T= , CM000666.1:g.122615110T=	GRCh37
NC_000004.10:g.122834560T=	NCBI36
NG_032042.1:g.8038A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.9+2626A= MANE Select	ENSP00000296511.5:n.9+2626A=
ENST00000296511.9:c.9+2626A=	ENSP00000296511.5:n.9+2626A=
ENST00000501272.6:c.9+2626A=	ENSP00000424106.1:n.9+2626A=
ENST00000506395.5:c.9+2626A=	ENSP00000421421.1:n.9+2626A=
ENST00000509016.5:n.130+2908A=
ENST00000511552.5:n.395+2626A=
ENST00000513428.5:n.174+2626A=
ENST00000513523.1:n.177+2626A=
ENST00000513728.1:c.9+2626A=	ENSP00000427135.1:n.9+2626A=
ENST00000515017.5:c.9+2626A=	ENSP00000424199.1:n.9+2626A=
NM_001154.3:c.9+2626A=	NP_001145.1:n.9+2626A=
XM_017008141.2:c.9+2626A=	XP_016863630.1:n.9+2626A=
NM_001154.4:c.9+2626A= MANE Select	NP_001145.1:n.9+2626A=