Canonical Allele Identifier: CA358037442

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121686350-T-G
• MyVariant Identifiers: chr4:g.122607505T>G (hg19) ; chr4:g.121686350T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686350T>G , CM000666.2:g.121686350T>G	GRCh38
NC_000004.11:g.122607505T>G , CM000666.1:g.122607505T>G	GRCh37
NC_000004.10:g.122826955T>G	NCBI36
NG_032042.1:g.15643A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.32A>C MANE Select	ENSP00000296511.5:p.Asp11Ala
ENST00000296511.9:c.32A>C	ENSP00000296511.5:p.Asp11Ala
ENST00000501272.6:c.10-2873A>C	ENSP00000424106.1:n.10-2873A>C
ENST00000506395.5:c.32A>C	ENSP00000421421.1:p.Asp11Ala
ENST00000509016.5:n.153A>C
ENST00000511552.5:n.418A>C
ENST00000513428.5:n.197A>C
ENST00000513523.1:n.200A>C
ENST00000513728.1:c.32A>C	ENSP00000427135.1:p.Asp11Ala
ENST00000515017.5:c.32A>C	ENSP00000424199.1:p.Asp11Ala
NM_001154.3:c.32A>C	NP_001145.1:p.Asp11Ala
XM_017008141.2:c.32A>C	XP_016863630.1:p.Asp11Ala
NM_001154.4:c.32A>C MANE Select	NP_001145.1:p.Asp11Ala