Canonical Allele Identifier: CA1732790075
Gene: SLC26A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767701_107767703delinsAAG , CM000669.2:g.107767701_107767703delinsAAG GRCh38
NC_000007.13:g.107408146_107408148delinsAAG , CM000669.1:g.107408146_107408148delinsAAG GRCh37
NC_000007.12:g.107195382_107195384delinsAAG NCBI36
NG_008046.1:g.40531_40533delinsCTT , LRG_683:g.40531_40533delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000340010.10:c.2206-59_2206-57delinsCTT MANE Select ENSP00000345873.5:n.2206-59_2206-57delinsCTT
ENST00000340010.9:c.2206-59_2206-57delinsCTT ENSP00000345873.5:n.2206-59_2206-57delinsCTT
ENST00000379083.7:c.*1763-59_*1763-57delinsCTT ENSP00000368375.3:n.*1763-59_*1763-57delinsCTT
NM_000111.2:c.2206-59_2206-57delinsCTT , LRG_683t1:c.2206-59_2206-57delinsCTT NP_000102.1:n.2206-59_2206-57delinsCTT
XM_011515867.1:c.2206-59_2206-57delinsCTT XP_011514169.1:n.2206-59_2206-57delinsCTT
NM_000111.3:c.2206-59_2206-57delinsCTT MANE Select NP_000102.1:n.2206-59_2206-57delinsCTT