Canonical Allele Identifier: CA1816658833

Gene: ANXA13

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123702593G= , CM000670.2:g.123702593G=	GRCh38
NC_000008.10:g.124714833G= , CM000670.1:g.124714833G=	GRCh37
NC_000008.9:g.124784014G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419625.6:c.186+49C= MANE Select	ENSP00000390809.1:n.186+49C=
ENST00000262219.10:c.309+49C=	ENSP00000262219.6:n.309+49C=
ENST00000419625.5:c.186+49C=	ENSP00000390809.1:n.186+49C=
ENST00000520519.1:c.99+49C=	ENSP00000429358.1:n.99+49C=
NM_001003954.1:c.309+49C=	NP_001003954.1:n.309+49C=
NM_004306.2:c.186+49C=	NP_004297.2:n.186+49C=
NM_001003954.2:c.309+49C=	NP_001003954.1:n.309+49C=
NM_004306.3:c.186+49C=	NP_004297.2:n.186+49C=
NM_004306.4:c.186+49C= MANE Select	NP_004297.2:n.186+49C=
NM_001003954.3:c.309+49C=	NP_001003954.1:n.309+49C=