Canonical Allele Identifier: CA2527141337

Gene: ANXA13

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123702521_123702522insAATTGGGACTAACTGTACATATGTAGC , CM000670.2:g.123702521_123702522insAATTGGGACTAACTGTACATATGTAGC	GRCh38
NC_000008.10:g.124714761_124714762insAATTGGGACTAACTGTACATATGTAGC , CM000670.1:g.124714761_124714762insAATTGGGACTAACTGTACATATGTAGC	GRCh37
NC_000008.9:g.124783942_124783943insAATTGGGACTAACTGTACATATGTAGC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000419625.6:c.186+120_186+121insGCTACATATGTACAGTTAGTCCCAATT MANE Select	ENSP00000390809.1:n.186+120_186+121insGCT...
ENST00000262219.10:c.309+120_309+121insGCTACATATGTACAGTTAGTCCCAATT	ENSP00000262219.6:n.309+120_309+121insGCT...
ENST00000419625.5:c.186+120_186+121insGCTACATATGTACAGTTAGTCCCAATT	ENSP00000390809.1:n.186+120_186+121insGCT...
ENST00000520519.1:c.99+120_99+121insGCTACATATGTACAGTTAGTCCCAATT	ENSP00000429358.1:n.99+120_99+121insGCTAC...
NM_001003954.1:c.309+120_309+121insGCTACATATGTACAGTTAGTCCCAATT	NP_001003954.1:n.309+120_309+121insGCTACA...
NM_004306.2:c.186+120_186+121insGCTACATATGTACAGTTAGTCCCAATT	NP_004297.2:n.186+120_186+121insGCTACATAT...
NM_001003954.2:c.309+120_309+121insGCTACATATGTACAGTTAGTCCCAATT	NP_001003954.1:n.309+120_309+121insGCTACA...
NM_004306.3:c.186+120_186+121insGCTACATATGTACAGTTAGTCCCAATT	NP_004297.2:n.186+120_186+121insGCTACATAT...
NM_004306.4:c.186+120_186+121insGCTACATATGTACAGTTAGTCCCAATT MANE Select	NP_004297.2:n.186+120_186+121insGCTACATAT...
NM_001003954.3:c.309+120_309+121insGCTACATATGTACAGTTAGTCCCAATT	NP_001003954.1:n.309+120_309+121insGCTACA...