Canonical Allele Identifier: CA786353264

Gene: ANXA5

Linked Data

• dbSNP Id: rs1305319583
• gnomAD v3: 4-121686471-AT-A
• gnomAD v4: 4-121686471-AT-A
• MyVariant Identifiers: chr4:g.122607627del (hg19) ; chr4:g.121686472del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686473del , CM000666.2:g.121686473del	GRCh38
NC_000004.11:g.122607628del , CM000666.1:g.122607628del	GRCh37
NC_000004.10:g.122827078del	NCBI36
NG_032042.1:g.15521del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-100del MANE Select	ENSP00000296511.5:n.10-100del
ENST00000296511.9:c.10-100del	ENSP00000296511.5:n.10-100del
ENST00000501272.6:c.10-2995del	ENSP00000424106.1:n.10-2995del
ENST00000506395.5:c.10-100del	ENSP00000421421.1:n.10-100del
ENST00000509016.5:n.131-100del
ENST00000511552.5:n.396-100del
ENST00000513428.5:n.175-100del
ENST00000513523.1:n.178-100del
ENST00000513728.1:c.10-100del	ENSP00000427135.1:n.10-100del
ENST00000515017.5:c.10-100del	ENSP00000424199.1:n.10-100del
NM_001154.3:c.10-100del	NP_001145.1:n.10-100del
XM_017008141.2:c.10-100del	XP_016863630.1:n.10-100del
NM_001154.4:c.10-100del MANE Select	NP_001145.1:n.10-100del