Canonical Allele Identifier: CA1489951952

Gene: ANXA5

Linked Data

• dbSNP Id: rs1724878196

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121685846_121685848dup , CM000666.2:g.121685846_121685848dup	GRCh38
NC_000004.11:g.122607001_122607003dup , CM000666.1:g.122607001_122607003dup	GRCh37
NC_000004.10:g.122826451_122826453dup	NCBI36
NG_032042.1:g.16146_16148dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+441_94+443dup MANE Select	ENSP00000296511.5:n.94+441_94+443dup
ENST00000296511.9:c.94+441_94+443dup	ENSP00000296511.5:n.94+441_94+443dup
ENST00000501272.6:c.10-2370_10-2368dup	ENSP00000424106.1:n.10-2370_10-2368dup
ENST00000506395.5:c.94+441_94+443dup	ENSP00000421421.1:n.94+441_94+443dup
ENST00000509016.5:n.215+441_215+443dup
ENST00000511552.5:n.480+441_480+443dup
ENST00000513428.5:n.259+441_259+443dup
ENST00000513523.1:n.262+441_262+443dup
ENST00000513728.1:c.94+441_94+443dup	ENSP00000427135.1:n.94+441_94+443dup
ENST00000515017.5:c.94+441_94+443dup	ENSP00000424199.1:n.94+441_94+443dup
NM_001154.3:c.94+441_94+443dup	NP_001145.1:n.94+441_94+443dup
XM_017008141.2:c.94+441_94+443dup	XP_016863630.1:n.94+441_94+443dup
NM_001154.4:c.94+441_94+443dup MANE Select	NP_001145.1:n.94+441_94+443dup