Canonical Allele Identifier: CA4867594

Gene: ANXA13

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.123735777C>G , CM000670.2:g.123735777C>G	GRCh38
NC_000008.10:g.124748017C>G , CM000670.1:g.124748017C>G	GRCh37
NC_000008.9:g.124817198C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004306.4:c.15+1543G>C MANE Select	NP_004297.2:n.15+1543G>C
ENST00000419625.6:c.15+1543G>C MANE Select	ENSP00000390809.1:n.15+1543G>C
NM_001003954.1:c.116G>C	NP_001003954.1:p.Gly39Ala
NM_001003954.2:c.116G>C	NP_001003954.1:p.Gly39Ala
NM_001003954.3:c.116G>C	NP_001003954.1:p.Gly39Ala
NM_004306.2:c.15+1543G>C	NP_004297.2:n.15+1543G>C
NM_004306.3:c.15+1543G>C	NP_004297.2:n.15+1543G>C
ENST00000262219.10:c.116G>C	ENSP00000262219.6:p.Gly39Ala
ENST00000419625.5:c.15+1543G>C	ENSP00000390809.1:n.15+1543G>C
XR_928607.1:n.152+15816C>G
XR_928607.3:n.323+15816C>G