Canonical Allele Identifier: CA1067431122

Gene: ANXA5

Linked Data

• dbSNP Id: rs1424725003
• gnomAD v3: 4-121686271-G-A
• gnomAD v4: 4-121686271-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686271G>A , CM000666.2:g.121686271G>A	GRCh38
NC_000004.11:g.122607426G>A , CM000666.1:g.122607426G>A	GRCh37
NC_000004.10:g.122826876G>A	NCBI36
NG_032042.1:g.15722C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+17C>T MANE Select	ENSP00000296511.5:n.94+17C>T
ENST00000296511.9:c.94+17C>T	ENSP00000296511.5:n.94+17C>T
ENST00000501272.6:c.10-2794C>T	ENSP00000424106.1:n.10-2794C>T
ENST00000506395.5:c.94+17C>T	ENSP00000421421.1:n.94+17C>T
ENST00000509016.5:n.215+17C>T
ENST00000511552.5:n.480+17C>T
ENST00000513428.5:n.259+17C>T
ENST00000513523.1:n.262+17C>T
ENST00000513728.1:c.94+17C>T	ENSP00000427135.1:n.94+17C>T
ENST00000515017.5:c.94+17C>T	ENSP00000424199.1:n.94+17C>T
NM_001154.3:c.94+17C>T	NP_001145.1:n.94+17C>T
XM_017008141.2:c.94+17C>T	XP_016863630.1:n.94+17C>T
NM_001154.4:c.94+17C>T MANE Select	NP_001145.1:n.94+17C>T