Canonical Allele Identifier: CA786349106

Gene: ANXA5

Linked Data

• dbSNP Id: rs1430977344
• gnomAD v3: 4-121679500-G-A
• gnomAD v4: 4-121679500-G-A
• MyVariant Identifiers: chr4:g.122600655G>A (hg19) ; chr4:g.121679500G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121679500G>A , CM000666.2:g.121679500G>A	GRCh38
NC_000004.11:g.122600655G>A , CM000666.1:g.122600655G>A	GRCh37
NC_000004.10:g.122820105G>A	NCBI36
NG_032042.1:g.22493C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.395-1006C>T MANE Select	ENSP00000296511.5:n.395-1006C>T
ENST00000296511.9:c.395-1006C>T	ENSP00000296511.5:n.395-1006C>T
ENST00000501272.6:c.215-1006C>T	ENSP00000424106.1:n.215-1006C>T
ENST00000506395.5:c.395-1006C>T	ENSP00000421421.1:n.395-1006C>T
ENST00000509016.5:n.516-1006C>T
ENST00000511552.5:n.781-1006C>T
ENST00000515017.5:c.95-1006C>T	ENSP00000424199.1:n.95-1006C>T
NM_001154.3:c.395-1006C>T	NP_001145.1:n.395-1006C>T
NM_001154.4:c.395-1006C>T MANE Select	NP_001145.1:n.395-1006C>T