Canonical Allele Identifier: CA104723069

Gene: ANXA5

Linked Data

• dbSNP Id: rs538867093
• gnomAD v3: 4-121685951-A-G
• gnomAD v4: 4-121685951-A-G
• MyVariant Identifiers: chr4:g.122607106A>G (hg19) ; chr4:g.121685951A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121685951A>G , CM000666.2:g.121685951A>G	GRCh38
NC_000004.11:g.122607106A>G , CM000666.1:g.122607106A>G	GRCh37
NC_000004.10:g.122826556A>G	NCBI36
NG_032042.1:g.16042T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.94+337T>C MANE Select	ENSP00000296511.5:n.94+337T>C
ENST00000296511.9:c.94+337T>C	ENSP00000296511.5:n.94+337T>C
ENST00000501272.6:c.10-2474T>C	ENSP00000424106.1:n.10-2474T>C
ENST00000506395.5:c.94+337T>C	ENSP00000421421.1:n.94+337T>C
ENST00000509016.5:n.215+337T>C
ENST00000511552.5:n.480+337T>C
ENST00000513428.5:n.259+337T>C
ENST00000513523.1:n.262+337T>C
ENST00000513728.1:c.94+337T>C	ENSP00000427135.1:n.94+337T>C
ENST00000515017.5:c.94+337T>C	ENSP00000424199.1:n.94+337T>C
NM_001154.3:c.94+337T>C	NP_001145.1:n.94+337T>C
XM_017008141.2:c.94+337T>C	XP_016863630.1:n.94+337T>C
NM_001154.4:c.94+337T>C MANE Select	NP_001145.1:n.94+337T>C