Canonical Allele Identifier: CA786353006

Gene: ANXA5

Linked Data

• dbSNP Id: rs1415446281
• gnomAD v3: 4-121686261-G-C
• gnomAD v4: 4-121686261-G-C
• MyVariant Identifiers: chr4:g.122607416G>C (hg19) ; chr4:g.121686261G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686261G>C , CM000666.2:g.121686261G>C	GRCh38
NC_000004.11:g.122607416G>C , CM000666.1:g.122607416G>C	GRCh37
NC_000004.10:g.122826866G>C	NCBI36
NG_032042.1:g.15732C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+27C>G MANE Select	ENSP00000296511.5:n.94+27C>G
ENST00000296511.9:c.94+27C>G	ENSP00000296511.5:n.94+27C>G
ENST00000501272.6:c.10-2784C>G	ENSP00000424106.1:n.10-2784C>G
ENST00000506395.5:c.94+27C>G	ENSP00000421421.1:n.94+27C>G
ENST00000509016.5:n.215+27C>G
ENST00000511552.5:n.480+27C>G
ENST00000513428.5:n.259+27C>G
ENST00000513523.1:n.262+27C>G
ENST00000513728.1:c.94+27C>G	ENSP00000427135.1:n.94+27C>G
ENST00000515017.5:c.94+27C>G	ENSP00000424199.1:n.94+27C>G
NM_001154.3:c.94+27C>G	NP_001145.1:n.94+27C>G
XM_017008141.2:c.94+27C>G	XP_016863630.1:n.94+27C>G
NM_001154.4:c.94+27C>G MANE Select	NP_001145.1:n.94+27C>G