Canonical Allele Identifier: CA4867596

Gene: ANXA13

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123735791G>T , CM000670.2:g.123735791G>T	GRCh38
NC_000008.10:g.124748031G>T , CM000670.1:g.124748031G>T	GRCh37
NC_000008.9:g.124817212G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004306.4:c.15+1529C>A MANE Select	NP_004297.2:n.15+1529C>A
ENST00000419625.6:c.15+1529C>A MANE Select	ENSP00000390809.1:n.15+1529C>A
NM_001003954.1:c.102C>A	NP_001003954.1:p.His34Gln
NM_001003954.2:c.102C>A	NP_001003954.1:p.His34Gln
NM_001003954.3:c.102C>A	NP_001003954.1:p.His34Gln
NM_004306.2:c.15+1529C>A	NP_004297.2:n.15+1529C>A
NM_004306.3:c.15+1529C>A	NP_004297.2:n.15+1529C>A
ENST00000262219.10:c.102C>A	ENSP00000262219.6:p.His34Gln
ENST00000419625.5:c.15+1529C>A	ENSP00000390809.1:n.15+1529C>A
XR_928607.1:n.152+15830G>T
XR_928607.3:n.323+15830G>T