Canonical Allele Identifier: CA1732790135
Gene: SLC26A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767763T= , CM000669.2:g.107767763T= GRCh38
NC_000007.13:g.107408208T= , CM000669.1:g.107408208T= GRCh37
NC_000007.12:g.107195444T= NCBI36
NG_008046.1:g.40471A= , LRG_683:g.40471A=

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2205+3A= MANE Select ENSP00000345873.5:n.2205+3A=
ENST00000340010.9:c.2205+3A= ENSP00000345873.5:n.2205+3A=
ENST00000379083.7:c.*1762+3A= ENSP00000368375.3:n.*1762+3A=
NM_000111.2:c.2205+3A= , LRG_683t1:c.2205+3A= NP_000102.1:n.2205+3A=
XM_011515867.1:c.2205+3A= XP_011514169.1:n.2205+3A=
NM_000111.3:c.2205+3A= MANE Select NP_000102.1:n.2205+3A=