Canonical Allele Identifier: CA649221440

Gene: ANXA5

Linked Data

• COSMIC: COSN19226460

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121693849A>C , CM000666.2:g.121693849A>C	GRCh38
NC_000004.11:g.122615004A>C , CM000666.1:g.122615004A>C	GRCh37
NC_000004.10:g.122834454A>C	NCBI36
NG_032042.1:g.8144T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.9+2732T>G MANE Select	ENSP00000296511.5:n.9+2732T>G
ENST00000296511.9:c.9+2732T>G	ENSP00000296511.5:n.9+2732T>G
ENST00000501272.6:c.9+2732T>G	ENSP00000424106.1:n.9+2732T>G
ENST00000506395.5:c.9+2732T>G	ENSP00000421421.1:n.9+2732T>G
ENST00000509016.5:n.130+3014T>G
ENST00000511552.5:n.395+2732T>G
ENST00000513428.5:n.174+2732T>G
ENST00000513523.1:n.177+2732T>G
ENST00000513728.1:c.9+2732T>G	ENSP00000427135.1:n.9+2732T>G
ENST00000515017.5:c.9+2732T>G	ENSP00000424199.1:n.9+2732T>G
NM_001154.3:c.9+2732T>G	NP_001145.1:n.9+2732T>G
XM_017008141.2:c.9+2732T>G	XP_016863630.1:n.9+2732T>G
NM_001154.4:c.9+2732T>G MANE Select	NP_001145.1:n.9+2732T>G