Canonical Allele Identifier: CA1732790046
Gene: SLC26A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767674_107767675delinsAG , CM000669.2:g.107767674_107767675delinsAG GRCh38
NC_000007.13:g.107408119_107408120delinsAG , CM000669.1:g.107408119_107408120delinsAG GRCh37
NC_000007.12:g.107195355_107195356delinsAG NCBI36
NG_008046.1:g.40559_40560delinsCT , LRG_683:g.40559_40560delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2206-31_2206-30delinsCT MANE Select ENSP00000345873.5:n.2206-31_2206-30delins...
ENST00000340010.9:c.2206-31_2206-30delinsCT ENSP00000345873.5:n.2206-31_2206-30delins...
ENST00000379083.7:c.*1763-31_*1763-30delinsCT ENSP00000368375.3:n.*1763-31_*1763-30deli...
NM_000111.2:c.2206-31_2206-30delinsCT , LRG_683t1:c.2206-31_2206-30delinsCT NP_000102.1:n.2206-31_2206-30delinsCT
XM_011515867.1:c.2206-31_2206-30delinsCT XP_011514169.1:n.2206-31_2206-30delinsCT
NM_000111.3:c.2206-31_2206-30delinsCT MANE Select NP_000102.1:n.2206-31_2206-30delinsCT