Canonical Allele Identifier: CA2684464226
Gene: SLC26A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767764dup , CM000669.2:g.107767764dup GRCh38
NC_000007.13:g.107408209dup , CM000669.1:g.107408209dup GRCh37
NC_000007.12:g.107195445dup NCBI36
NG_008046.1:g.40470dup , LRG_683:g.40470dup

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2205+2dup MANE Select ENSP00000345873.5:n.2205+2dup
ENST00000340010.9:c.2205+2dup ENSP00000345873.5:n.2205+2dup
ENST00000379083.7:c.*1762+2dup ENSP00000368375.3:n.*1762+2dup
NM_000111.2:c.2205+2dup , LRG_683t1:c.2205+2dup NP_000102.1:n.2205+2dup
XM_011515867.1:c.2205+2dup XP_011514169.1:n.2205+2dup
NM_000111.3:c.2205+2dup MANE Select NP_000102.1:n.2205+2dup