Canonical Allele Identifier: CA368849511
Gene: SLC26A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767773G>C , CM000669.2:g.107767773G>C GRCh38
NC_000007.13:g.107408218G>C , CM000669.1:g.107408218G>C GRCh37
NC_000007.12:g.107195454G>C NCBI36
NG_008046.1:g.40461C>G , LRG_683:g.40461C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2198C>G MANE Select ENSP00000345873.5:p.Pro733Arg
ENST00000340010.9:c.2198C>G ENSP00000345873.5:p.Pro733Arg
ENST00000379083.7:c.*1755C>G ENSP00000368375.3:n.*1755C>G
NM_000111.2:c.2198C>G , LRG_683t1:c.2198C>G NP_000102.1:p.Pro733Arg
XM_011515867.1:c.2198C>G XP_011514169.1:p.Pro733Arg
NM_000111.3:c.2198C>G MANE Select NP_000102.1:p.Pro733Arg