Canonical Allele Identifier: CA1732787387
Gene: SLC26A3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779588A= , CM000669.2:g.107779588A= GRCh38
NC_000007.13:g.107420033A= , CM000669.1:g.107420033A= GRCh37
NC_000007.12:g.107207269A= NCBI36
NG_008046.1:g.28646T= , LRG_683:g.28646T=

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.1407+80T= MANE Select ENSP00000345873.5:n.1407+80T=
ENST00000340010.9:c.1407+80T= ENSP00000345873.5:n.1407+80T=
ENST00000379083.7:c.*1198+80T= ENSP00000368375.3:n.*1198+80T=
NM_000111.2:c.1407+80T= , LRG_683t1:c.1407+80T= NP_000102.1:n.1407+80T=
XM_011515867.1:c.1407+80T= XP_011514169.1:n.1407+80T=
NM_000111.3:c.1407+80T= MANE Select NP_000102.1:n.1407+80T=
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