Canonical Allele Identifier: CA358037209

Gene: ANXA5

Linked Data

• MyVariant Identifiers: chr4:g.122607451T>C (hg19) ; chr4:g.121686296T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686296T>C , CM000666.2:g.121686296T>C	GRCh38
NC_000004.11:g.122607451T>C , CM000666.1:g.122607451T>C	GRCh37
NC_000004.10:g.122826901T>C	NCBI36
NG_032042.1:g.15697A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.86A>G MANE Select	ENSP00000296511.5:p.Lys29Arg
ENST00000296511.9:c.86A>G	ENSP00000296511.5:p.Lys29Arg
ENST00000501272.6:c.10-2819A>G	ENSP00000424106.1:n.10-2819A>G
ENST00000506395.5:c.86A>G	ENSP00000421421.1:p.Lys29Arg
ENST00000509016.5:n.207A>G
ENST00000511552.5:n.472A>G
ENST00000513428.5:n.251A>G
ENST00000513523.1:n.254A>G
ENST00000513728.1:c.86A>G	ENSP00000427135.1:p.Lys29Arg
ENST00000515017.5:c.86A>G	ENSP00000424199.1:p.Lys29Arg
NM_001154.3:c.86A>G	NP_001145.1:p.Lys29Arg
XM_017008141.2:c.86A>G	XP_016863630.1:p.Lys29Arg
NM_001154.4:c.86A>G MANE Select	NP_001145.1:p.Lys29Arg