Canonical Allele Identifier: CA1816658793
Gene: ANXA13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.123702529_123702530delinsTG , CM000670.2:g.123702529_123702530delinsTG GRCh38
NC_000008.10:g.124714769_124714770delinsTG , CM000670.1:g.124714769_124714770delinsTG GRCh37
NC_000008.9:g.124783950_124783951delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000419625.6:c.186+112_186+113delinsCA MANE Select ENSP00000390809.1:n.186+112_186+113delinsCA
ENST00000262219.10:c.309+112_309+113delinsCA ENSP00000262219.6:n.309+112_309+113delinsCA
ENST00000419625.5:c.186+112_186+113delinsCA ENSP00000390809.1:n.186+112_186+113delinsCA
ENST00000520519.1:c.99+112_99+113delinsCA ENSP00000429358.1:n.99+112_99+113delinsCA
NM_001003954.1:c.309+112_309+113delinsCA NP_001003954.1:n.309+112_309+113delinsCA
NM_004306.2:c.186+112_186+113delinsCA NP_004297.2:n.186+112_186+113delinsCA
NM_001003954.2:c.309+112_309+113delinsCA NP_001003954.1:n.309+112_309+113delinsCA
NM_004306.3:c.186+112_186+113delinsCA NP_004297.2:n.186+112_186+113delinsCA
NM_004306.4:c.186+112_186+113delinsCA MANE Select NP_004297.2:n.186+112_186+113delinsCA
NM_001003954.3:c.309+112_309+113delinsCA NP_001003954.1:n.309+112_309+113delinsCA
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