Canonical Allele Identifier: CA2579243434

Gene: ANXA13

Linked Data

• gnomAD v4: 8-123702550-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123702553del , CM000670.2:g.123702553del	GRCh38
NC_000008.10:g.124714793del , CM000670.1:g.124714793del	GRCh37
NC_000008.9:g.124783974del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000419625.6:c.186+91del MANE Select	ENSP00000390809.1:n.186+91del
ENST00000262219.10:c.309+91del	ENSP00000262219.6:n.309+91del
ENST00000419625.5:c.186+91del	ENSP00000390809.1:n.186+91del
ENST00000520519.1:c.99+91del	ENSP00000429358.1:n.99+91del
NM_001003954.1:c.309+91del	NP_001003954.1:n.309+91del
NM_004306.2:c.186+91del	NP_004297.2:n.186+91del
NM_001003954.2:c.309+91del	NP_001003954.1:n.309+91del
NM_004306.3:c.186+91del	NP_004297.2:n.186+91del
NM_004306.4:c.186+91del MANE Select	NP_004297.2:n.186+91del
NM_001003954.3:c.309+91del	NP_001003954.1:n.309+91del