Canonical Allele Identifier: CA368849497
Gene: SLC26A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767767T>A , CM000669.2:g.107767767T>A GRCh38
NC_000007.13:g.107408212T>A , CM000669.1:g.107408212T>A GRCh37
NC_000007.12:g.107195448T>A NCBI36
NG_008046.1:g.40467A>T , LRG_683:g.40467A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2204A>T MANE Select ENSP00000345873.5:p.Gln735Leu
ENST00000340010.9:c.2204A>T ENSP00000345873.5:p.Gln735Leu
ENST00000379083.7:c.*1761A>T ENSP00000368375.3:n.*1761A>T
NM_000111.2:c.2204A>T , LRG_683t1:c.2204A>T NP_000102.1:p.Gln735Leu
XM_011515867.1:c.2204A>T XP_011514169.1:p.Gln735Leu
NM_000111.3:c.2204A>T MANE Select NP_000102.1:p.Gln735Leu