Canonical Allele Identifier: CA1816658805

Gene: ANXA13

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123702559T= , CM000670.2:g.123702559T=	GRCh38
NC_000008.10:g.124714799T= , CM000670.1:g.124714799T=	GRCh37
NC_000008.9:g.124783980T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419625.6:c.186+83A= MANE Select	ENSP00000390809.1:n.186+83A=
ENST00000262219.10:c.309+83A=	ENSP00000262219.6:n.309+83A=
ENST00000419625.5:c.186+83A=	ENSP00000390809.1:n.186+83A=
ENST00000520519.1:c.99+83A=	ENSP00000429358.1:n.99+83A=
NM_001003954.1:c.309+83A=	NP_001003954.1:n.309+83A=
NM_004306.2:c.186+83A=	NP_004297.2:n.186+83A=
NM_001003954.2:c.309+83A=	NP_001003954.1:n.309+83A=
NM_004306.3:c.186+83A=	NP_004297.2:n.186+83A=
NM_004306.4:c.186+83A= MANE Select	NP_004297.2:n.186+83A=
NM_001003954.3:c.309+83A=	NP_001003954.1:n.309+83A=