Canonical Allele Identifier: CA1732787534
Gene: SLC26A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779691A= , CM000669.2:g.107779691A= GRCh38
NC_000007.13:g.107420136A= , CM000669.1:g.107420136A= GRCh37
NC_000007.12:g.107207372A= NCBI36
NG_008046.1:g.28543T= , LRG_683:g.28543T=

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.1384T= MANE Select ENSP00000345873.5:p.Trp462=
ENST00000340010.9:c.1384T= ENSP00000345873.5:p.Trp462=
ENST00000379083.7:c.*1175T= ENSP00000368375.3:n.*1175T=
NM_000111.2:c.1384T= , LRG_683t1:c.1384T= NP_000102.1:p.Trp462=
XM_011515867.1:c.1384T= XP_011514169.1:p.Trp462=
NM_000111.3:c.1384T= MANE Select NP_000102.1:p.Trp462=