Canonical Allele Identifier: CA358037284

Gene: ANXA5

Linked Data

• dbSNP Id: rs1578446752
• MyVariant Identifiers: chr4:g.122607471T>A (hg19) ; chr4:g.121686316T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686316T>A , CM000666.2:g.121686316T>A	GRCh38
NC_000004.11:g.122607471T>A , CM000666.1:g.122607471T>A	GRCh37
NC_000004.10:g.122826921T>A	NCBI36
NG_032042.1:g.15677A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.66A>T MANE Select	ENSP00000296511.5:p.Glu22Asp
ENST00000296511.9:c.66A>T	ENSP00000296511.5:p.Glu22Asp
ENST00000501272.6:c.10-2839A>T	ENSP00000424106.1:n.10-2839A>T
ENST00000506395.5:c.66A>T	ENSP00000421421.1:p.Glu22Asp
ENST00000509016.5:n.187A>T
ENST00000511552.5:n.452A>T
ENST00000513428.5:n.231A>T
ENST00000513523.1:n.234A>T
ENST00000513728.1:c.66A>T	ENSP00000427135.1:p.Glu22Asp
ENST00000515017.5:c.66A>T	ENSP00000424199.1:p.Glu22Asp
NM_001154.3:c.66A>T	NP_001145.1:p.Glu22Asp
XM_017008141.2:c.66A>T	XP_016863630.1:p.Glu22Asp
NM_001154.4:c.66A>T MANE Select	NP_001145.1:p.Glu22Asp