Canonical Allele Identifier: CA440911902

Gene: ANXA5

Linked Data

• MyVariant Identifiers: chr4:g.122607519T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686364T>C , CM000666.2:g.121686364T>C	GRCh38
NC_000004.11:g.122607519T>C , CM000666.1:g.122607519T>C	GRCh37
NC_000004.10:g.122826969T>C	NCBI36
NG_032042.1:g.15629A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.18A>G MANE Select	ENSP00000296511.5:p.Arg6=
ENST00000296511.9:c.18A>G	ENSP00000296511.5:p.Arg6=
ENST00000501272.6:c.10-2887A>G	ENSP00000424106.1:n.10-2887A>G
ENST00000506395.5:c.18A>G	ENSP00000421421.1:p.Arg6=
ENST00000509016.5:n.139A>G
ENST00000511552.5:n.404A>G
ENST00000513428.5:n.183A>G
ENST00000513523.1:n.186A>G
ENST00000513728.1:c.18A>G	ENSP00000427135.1:p.Arg6=
ENST00000515017.5:c.18A>G	ENSP00000424199.1:p.Arg6=
NM_001154.3:c.18A>G	NP_001145.1:p.Arg6=
XM_017008141.2:c.18A>G	XP_016863630.1:p.Arg6=
NM_001154.4:c.18A>G MANE Select	NP_001145.1:p.Arg6=