Canonical Allele Identifier: CA1732787489

Gene: SLC26A3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107779673C= , CM000669.2:g.107779673C=	GRCh38
NC_000007.13:g.107420118C= , CM000669.1:g.107420118C=	GRCh37
NC_000007.12:g.107207354C=	NCBI36
NG_008046.1:g.28561G= , LRG_683:g.28561G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000340010.10:c.1402G= MANE Select	ENSP00000345873.5:p.Asp468=
ENST00000340010.9:c.1402G=	ENSP00000345873.5:p.Asp468=
ENST00000379083.7:c.*1193G=	ENSP00000368375.3:n.*1193G=
NM_000111.2:c.1402G= , LRG_683t1:c.1402G=	NP_000102.1:p.Asp468=
XM_011515867.1:c.1402G=	XP_011514169.1:p.Asp468=
NM_000111.3:c.1402G= MANE Select	NP_000102.1:p.Asp468=