Canonical Allele Identifier: CA1732787223
Gene: SLC26A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779429G= , CM000669.2:g.107779429G= GRCh38
NC_000007.13:g.107419874G= , CM000669.1:g.107419874G= GRCh37
NC_000007.12:g.107207110G= NCBI36
NG_008046.1:g.28805C= , LRG_683:g.28805C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340010.10:c.1407+239C= MANE Select ENSP00000345873.5:n.1407+239C=
ENST00000340010.9:c.1407+239C= ENSP00000345873.5:n.1407+239C=
ENST00000379083.7:c.*1198+239C= ENSP00000368375.3:n.*1198+239C=
NM_000111.2:c.1407+239C= , LRG_683t1:c.1407+239C= NP_000102.1:n.1407+239C=
XM_011515867.1:c.1407+239C= XP_011514169.1:n.1407+239C=
NM_000111.3:c.1407+239C= MANE Select NP_000102.1:n.1407+239C=