Canonical Allele Identifier: CA1816658756
Gene: ANXA13 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.123702436A= , CM000670.2:g.123702436A= GRCh38
NC_000008.10:g.124714676A= , CM000670.1:g.124714676A= GRCh37
NC_000008.9:g.124783857A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419625.6:c.186+206T= MANE Select ENSP00000390809.1:n.186+206T=
ENST00000262219.10:c.309+206T= ENSP00000262219.6:n.309+206T=
ENST00000419625.5:c.186+206T= ENSP00000390809.1:n.186+206T=
ENST00000520519.1:c.99+206T= ENSP00000429358.1:n.99+206T=
NM_001003954.1:c.309+206T= NP_001003954.1:n.309+206T=
NM_004306.2:c.186+206T= NP_004297.2:n.186+206T=
NM_001003954.2:c.309+206T= NP_001003954.1:n.309+206T=
NM_004306.3:c.186+206T= NP_004297.2:n.186+206T=
NM_004306.4:c.186+206T= MANE Select NP_004297.2:n.186+206T=
NM_001003954.3:c.309+206T= NP_001003954.1:n.309+206T=
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