Canonical Allele Identifier: CA1732787485
Gene: SLC26A3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779673_107779675delinsCAT , CM000669.2:g.107779673_107779675delinsCAT GRCh38
NC_000007.13:g.107420118_107420120delinsCAT , CM000669.1:g.107420118_107420120delinsCAT GRCh37
NC_000007.12:g.107207354_107207356delinsCAT NCBI36
NG_008046.1:g.28559_28561delinsATG , LRG_683:g.28559_28561delinsATG

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.1400_1402delinsATG MANE Select ENSP00000345873.5:p.Tyr467=
ENST00000340010.9:c.1400_1402delinsATG ENSP00000345873.5:p.Tyr467=
ENST00000379083.7:c.*1191_*1193delinsATG ENSP00000368375.3:n.*1191_*1193delinsATG
NM_000111.2:c.1400_1402delinsATG , LRG_683t1:c.1400_1402delinsATG NP_000102.1:p.Tyr467=
XM_011515867.1:c.1400_1402delinsATG XP_011514169.1:p.Tyr467=
NM_000111.3:c.1400_1402delinsATG MANE Select NP_000102.1:p.Tyr467=
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