Canonical Allele Identifier: CA1732790049
Gene: SLC26A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767675G= , CM000669.2:g.107767675G= GRCh38
NC_000007.13:g.107408120G= , CM000669.1:g.107408120G= GRCh37
NC_000007.12:g.107195356G= NCBI36
NG_008046.1:g.40559C= , LRG_683:g.40559C=

Transcript Alleles

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