Canonical Allele Identifier: CA1489952224

Gene: ANXA5

Linked Data

• dbSNP Id: rs1724891258
• gnomAD v4: 4-121686402-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686403dup , CM000666.2:g.121686403dup	GRCh38
NC_000004.11:g.122607558dup , CM000666.1:g.122607558dup	GRCh37
NC_000004.10:g.122827008dup	NCBI36
NG_032042.1:g.15590dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-31dup MANE Select	ENSP00000296511.5:n.10-31dup
ENST00000296511.9:c.10-31dup	ENSP00000296511.5:n.10-31dup
ENST00000501272.6:c.10-2926dup	ENSP00000424106.1:n.10-2926dup
ENST00000506395.5:c.10-31dup	ENSP00000421421.1:n.10-31dup
ENST00000509016.5:n.131-31dup
ENST00000511552.5:n.396-31dup
ENST00000513428.5:n.175-31dup
ENST00000513523.1:n.178-31dup
ENST00000513728.1:c.10-31dup	ENSP00000427135.1:n.10-31dup
ENST00000515017.5:c.10-31dup	ENSP00000424199.1:n.10-31dup
NM_001154.3:c.10-31dup	NP_001145.1:n.10-31dup
XM_017008141.2:c.10-31dup	XP_016863630.1:n.10-31dup
NM_001154.4:c.10-31dup MANE Select	NP_001145.1:n.10-31dup