Canonical Allele Identifier: CA1732790068
Gene: SLC26A3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767695T= , CM000669.2:g.107767695T= GRCh38
NC_000007.13:g.107408140T= , CM000669.1:g.107408140T= GRCh37
NC_000007.12:g.107195376T= NCBI36
NG_008046.1:g.40539A= , LRG_683:g.40539A=

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2206-51A= MANE Select ENSP00000345873.5:n.2206-51A=
ENST00000340010.9:c.2206-51A= ENSP00000345873.5:n.2206-51A=
ENST00000379083.7:c.*1763-51A= ENSP00000368375.3:n.*1763-51A=
NM_000111.2:c.2206-51A= , LRG_683t1:c.2206-51A= NP_000102.1:n.2206-51A=
XM_011515867.1:c.2206-51A= XP_011514169.1:n.2206-51A=
NM_000111.3:c.2206-51A= MANE Select NP_000102.1:n.2206-51A=
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