Canonical Allele Identifier: CA440911833

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121686307-C-T
• MyVariant Identifiers: chr4:g.122607462C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686307C>T , CM000666.2:g.121686307C>T	GRCh38
NC_000004.11:g.122607462C>T , CM000666.1:g.122607462C>T	GRCh37
NC_000004.10:g.122826912C>T	NCBI36
NG_032042.1:g.15686G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.75G>A MANE Select	ENSP00000296511.5:p.Arg25=
ENST00000296511.9:c.75G>A	ENSP00000296511.5:p.Arg25=
ENST00000501272.6:c.10-2830G>A	ENSP00000424106.1:n.10-2830G>A
ENST00000506395.5:c.75G>A	ENSP00000421421.1:p.Arg25=
ENST00000509016.5:n.196G>A
ENST00000511552.5:n.461G>A
ENST00000513428.5:n.240G>A
ENST00000513523.1:n.243G>A
ENST00000513728.1:c.75G>A	ENSP00000427135.1:p.Arg25=
ENST00000515017.5:c.75G>A	ENSP00000424199.1:p.Arg25=
NM_001154.3:c.75G>A	NP_001145.1:p.Arg25=
XM_017008141.2:c.75G>A	XP_016863630.1:p.Arg25=
NM_001154.4:c.75G>A MANE Select	NP_001145.1:p.Arg25=