Canonical Allele Identifier: CA104731739

Gene: ANXA5

Linked Data

• dbSNP Id: rs566485727
• gnomAD v2: 4-122618037-T-G
• gnomAD v3: 4-121696882-T-G
• gnomAD v4: 4-121696882-T-G
• MyVariant Identifiers: chr4:g.122618037T>G (hg19) ; chr4:g.121696882T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696882T>G , CM000666.2:g.121696882T>G	GRCh38
NC_000004.11:g.122618037T>G , CM000666.1:g.122618037T>G	GRCh37
NC_000004.10:g.122837487T>G	NCBI36
NG_032042.1:g.5111A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.-55A>C MANE Select	ENSP00000296511.5:n.-55A>C
ENST00000296511.9:c.-55A>C	ENSP00000296511.5:n.-55A>C
ENST00000501272.6:c.-55A>C	ENSP00000424106.1:n.-55A>C
ENST00000506395.5:c.-55A>C	ENSP00000421421.1:n.-55A>C
ENST00000509016.5:n.111A>C
ENST00000511552.5:n.94A>C
ENST00000513428.5:n.111A>C
ENST00000513523.1:n.114A>C
ENST00000513728.1:c.-55A>C	ENSP00000427135.1:n.-55A>C
ENST00000515017.5:c.-55A>C	ENSP00000424199.1:n.-55A>C
NM_001154.3:c.-55A>C	NP_001145.1:n.-55A>C
XM_017008141.2:c.-55A>C	XP_016863630.1:n.-55A>C
NM_001154.4:c.-55A>C MANE Select	NP_001145.1:n.-55A>C