Canonical Allele Identifier: CA2840007000
Gene: SLC26A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779773dup , CM000669.2:g.107779773dup GRCh38
NC_000007.13:g.107420218dup , CM000669.1:g.107420218dup GRCh37
NC_000007.12:g.107207454dup NCBI36
NG_008046.1:g.28465dup , LRG_683:g.28465dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000340010.10:c.1312-6dup MANE Select ENSP00000345873.5:n.1312-6dup
ENST00000340010.9:c.1312-6dup ENSP00000345873.5:n.1312-6dup
ENST00000379083.7:c.*1103-6dup ENSP00000368375.3:n.*1103-6dup
NM_000111.2:c.1312-6dup , LRG_683t1:c.1312-6dup NP_000102.1:n.1312-6dup
XM_011515867.1:c.1312-6dup XP_011514169.1:n.1312-6dup
NM_000111.3:c.1312-6dup MANE Select NP_000102.1:n.1312-6dup