Canonical Allele Identifier: CA1816658732
Gene: ANXA13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.123702373_123702404delinsTAAGTGAAAAAAAGACTAGGGTCTTCATAGAA , CM000670.2:g.123702373_123702404delinsTAAGTGAAAAAAAGACTAGGGTCTTCATAGAA GRCh38
NC_000008.10:g.124714613_124714644delinsTAAGTGAAAAAAAGACTAGGGTCTTCATAGAA , CM000670.1:g.124714613_124714644delinsTAAGTGAAAAAAAGACTAGGGTCTTCATAGAA GRCh37
NC_000008.9:g.124783794_124783825delinsTAAGTGAAAAAAAGACTAGGGTCTTCATAGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000419625.6:c.186+238_186+269delinsTTCTATGAAGACCCTAGTCTTTTTTTCACTTA MANE Select ENSP00000390809.1:n.186+238_186+269delinsTTCTATGAAGACCCTAGTCT...
ENST00000262219.10:c.309+238_309+269delinsTTCTATGAAGACCCTAGTCTTTTTTTCACTTA ENSP00000262219.6:n.309+238_309+269delinsTTCTATGAAGACCCTAGTCT...
ENST00000419625.5:c.186+238_186+269delinsTTCTATGAAGACCCTAGTCTTTTTTTCACTTA ENSP00000390809.1:n.186+238_186+269delinsTTCTATGAAGACCCTAGTCT...
ENST00000520519.1:c.99+238_99+269delinsTTCTATGAAGACCCTAGTCTTTTTTTCACTTA ENSP00000429358.1:n.99+238_99+269delinsTTCTATGAAGACCCTAGTCTTT...
NM_001003954.1:c.309+238_309+269delinsTTCTATGAAGACCCTAGTCTTTTTTTCACTTA NP_001003954.1:n.309+238_309+269delinsTTCTATGAAGACCCTAGTCTTTT...
NM_004306.2:c.186+238_186+269delinsTTCTATGAAGACCCTAGTCTTTTTTTCACTTA NP_004297.2:n.186+238_186+269delinsTTCTATGAAGACCCTAGTCTTTTTTT...
NM_001003954.2:c.309+238_309+269delinsTTCTATGAAGACCCTAGTCTTTTTTTCACTTA NP_001003954.1:n.309+238_309+269delinsTTCTATGAAGACCCTAGTCTTTT...
NM_004306.3:c.186+238_186+269delinsTTCTATGAAGACCCTAGTCTTTTTTTCACTTA NP_004297.2:n.186+238_186+269delinsTTCTATGAAGACCCTAGTCTTTTTTT...
NM_004306.4:c.186+238_186+269delinsTTCTATGAAGACCCTAGTCTTTTTTTCACTTA MANE Select NP_004297.2:n.186+238_186+269delinsTTCTATGAAGACCCTAGTCTTTTTTT...
NM_001003954.3:c.309+238_309+269delinsTTCTATGAAGACCCTAGTCTTTTTTTCACTTA NP_001003954.1:n.309+238_309+269delinsTTCTATGAAGACCCTAGTCTTTT...