Canonical Allele Identifier: CA2688458612

Gene: ANXA13

Linked Data

• gnomAD v4: 8-123702519-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123702523del , CM000670.2:g.123702523del	GRCh38
NC_000008.10:g.124714763del , CM000670.1:g.124714763del	GRCh37
NC_000008.9:g.124783944del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000419625.6:c.186+122del MANE Select	ENSP00000390809.1:n.186+122del
ENST00000262219.10:c.309+122del	ENSP00000262219.6:n.309+122del
ENST00000419625.5:c.186+122del	ENSP00000390809.1:n.186+122del
ENST00000520519.1:c.99+122del	ENSP00000429358.1:n.99+122del
NM_001003954.1:c.309+122del	NP_001003954.1:n.309+122del
NM_004306.2:c.186+122del	NP_004297.2:n.186+122del
NM_001003954.2:c.309+122del	NP_001003954.1:n.309+122del
NM_004306.3:c.186+122del	NP_004297.2:n.186+122del
NM_004306.4:c.186+122del MANE Select	NP_004297.2:n.186+122del
NM_001003954.3:c.309+122del	NP_001003954.1:n.309+122del