Canonical Allele Identifier: CA3063040

Gene: ANXA5

Linked Data

• dbSNP Id: rs773115198
• ExAC: 4:122607449 C / G
• gnomAD v2: 4-122607449-C-G
• gnomAD v3: 4-121686294-C-G
• gnomAD v4: 4-121686294-C-G
• MyVariant Identifiers: chr4:g.122607449C>G (hg19) ; chr4:g.121686294C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686294C>G , CM000666.2:g.121686294C>G	GRCh38
NC_000004.11:g.122607449C>G , CM000666.1:g.122607449C>G	GRCh37
NC_000004.10:g.122826899C>G	NCBI36
NG_032042.1:g.15699G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.88G>C MANE Select	ENSP00000296511.5:p.Gly30Arg
ENST00000296511.9:c.88G>C	ENSP00000296511.5:p.Gly30Arg
ENST00000501272.6:c.10-2817G>C	ENSP00000424106.1:n.10-2817G>C
ENST00000506395.5:c.88G>C	ENSP00000421421.1:p.Gly30Arg
ENST00000509016.5:n.209G>C
ENST00000511552.5:n.474G>C
ENST00000513428.5:n.253G>C
ENST00000513523.1:n.256G>C
ENST00000513728.1:c.88G>C	ENSP00000427135.1:p.Gly30Arg
ENST00000515017.5:c.88G>C	ENSP00000424199.1:p.Gly30Arg
NM_001154.3:c.88G>C	NP_001145.1:p.Gly30Arg
XM_017008141.2:c.88G>C	XP_016863630.1:p.Gly30Arg
NM_001154.4:c.88G>C MANE Select	NP_001145.1:p.Gly30Arg