Canonical Allele Identifier: CA2671937293

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121686504-ACCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686506_121686508del , CM000666.2:g.121686506_121686508del	GRCh38
NC_000004.11:g.122607661_122607663del , CM000666.1:g.122607661_122607663del	GRCh37
NC_000004.10:g.122827111_122827113del	NCBI36
NG_032042.1:g.15486_15488del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-135_10-133del MANE Select	ENSP00000296511.5:n.10-135_10-133del
ENST00000296511.9:c.10-135_10-133del	ENSP00000296511.5:n.10-135_10-133del
ENST00000501272.6:c.10-3030_10-3028del	ENSP00000424106.1:n.10-3030_10-3028del
ENST00000506395.5:c.10-135_10-133del	ENSP00000421421.1:n.10-135_10-133del
ENST00000509016.5:n.131-135_131-133del
ENST00000511552.5:n.396-135_396-133del
ENST00000513428.5:n.175-135_175-133del
ENST00000513523.1:n.178-135_178-133del
ENST00000513728.1:c.10-135_10-133del	ENSP00000427135.1:n.10-135_10-133del
ENST00000515017.5:c.10-135_10-133del	ENSP00000424199.1:n.10-135_10-133del
NM_001154.3:c.10-135_10-133del	NP_001145.1:n.10-135_10-133del
XM_017008141.2:c.10-135_10-133del	XP_016863630.1:n.10-135_10-133del
NM_001154.4:c.10-135_10-133del MANE Select	NP_001145.1:n.10-135_10-133del