Canonical Allele Identifier: CA1732787504
Gene: SLC26A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779684T= , CM000669.2:g.107779684T= GRCh38
NC_000007.13:g.107420129T= , CM000669.1:g.107420129T= GRCh37
NC_000007.12:g.107207365T= NCBI36
NG_008046.1:g.28550A= , LRG_683:g.28550A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340010.10:c.1391A= MANE Select ENSP00000345873.5:p.Lys464=
ENST00000340010.9:c.1391A= ENSP00000345873.5:p.Lys464=
ENST00000379083.7:c.*1182A= ENSP00000368375.3:n.*1182A=
NM_000111.2:c.1391A= , LRG_683t1:c.1391A= NP_000102.1:p.Lys464=
XM_011515867.1:c.1391A= XP_011514169.1:p.Lys464=
NM_000111.3:c.1391A= MANE Select NP_000102.1:p.Lys464=