Canonical Allele Identifier: CA1732787529
Gene: SLC26A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779690C= , CM000669.2:g.107779690C= GRCh38
NC_000007.13:g.107420135C= , CM000669.1:g.107420135C= GRCh37
NC_000007.12:g.107207371C= NCBI36
NG_008046.1:g.28544G= , LRG_683:g.28544G=

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.1385G= MANE Select ENSP00000345873.5:p.Trp462=
ENST00000340010.9:c.1385G= ENSP00000345873.5:p.Trp462=
ENST00000379083.7:c.*1176G= ENSP00000368375.3:n.*1176G=
NM_000111.2:c.1385G= , LRG_683t1:c.1385G= NP_000102.1:p.Trp462=
XM_011515867.1:c.1385G= XP_011514169.1:p.Trp462=
NM_000111.3:c.1385G= MANE Select NP_000102.1:p.Trp462=