Canonical Allele Identifier: CA104723222

Gene: ANXA5

Linked Data

• dbSNP Id: rs1023610233
• MyVariant Identifiers: chr4:g.122607279A>T (hg19) ; chr4:g.121686124A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686124A>T , CM000666.2:g.121686124A>T	GRCh38
NC_000004.11:g.122607279A>T , CM000666.1:g.122607279A>T	GRCh37
NC_000004.10:g.122826729A>T	NCBI36
NG_032042.1:g.15869T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+164T>A MANE Select	ENSP00000296511.5:n.94+164T>A
ENST00000296511.9:c.94+164T>A	ENSP00000296511.5:n.94+164T>A
ENST00000501272.6:c.10-2647T>A	ENSP00000424106.1:n.10-2647T>A
ENST00000506395.5:c.94+164T>A	ENSP00000421421.1:n.94+164T>A
ENST00000509016.5:n.215+164T>A
ENST00000511552.5:n.480+164T>A
ENST00000513428.5:n.259+164T>A
ENST00000513523.1:n.262+164T>A
ENST00000513728.1:c.94+164T>A	ENSP00000427135.1:n.94+164T>A
ENST00000515017.5:c.94+164T>A	ENSP00000424199.1:n.94+164T>A
NM_001154.3:c.94+164T>A	NP_001145.1:n.94+164T>A
XM_017008141.2:c.94+164T>A	XP_016863630.1:n.94+164T>A
NM_001154.4:c.94+164T>A MANE Select	NP_001145.1:n.94+164T>A