Canonical Allele Identifier: CA1732787385

Gene: SLC26A3

Linked Data

• dbSNP Id: rs1794182715
• gnomAD v4: 7-107779585-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107779585T>C , CM000669.2:g.107779585T>C	GRCh38
NC_000007.13:g.107420030T>C , CM000669.1:g.107420030T>C	GRCh37
NC_000007.12:g.107207266T>C	NCBI36
NG_008046.1:g.28649A>G , LRG_683:g.28649A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000340010.10:c.1407+83A>G MANE Select	ENSP00000345873.5:n.1407+83A>G
ENST00000340010.9:c.1407+83A>G	ENSP00000345873.5:n.1407+83A>G
ENST00000379083.7:c.*1198+83A>G	ENSP00000368375.3:n.*1198+83A>G
NM_000111.2:c.1407+83A>G , LRG_683t1:c.1407+83A>G	NP_000102.1:n.1407+83A>G
XM_011515867.1:c.1407+83A>G	XP_011514169.1:n.1407+83A>G
NM_000111.3:c.1407+83A>G MANE Select	NP_000102.1:n.1407+83A>G