Canonical Allele Identifier: CA1732787135

Gene: SLC26A3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107779335C= , CM000669.2:g.107779335C=	GRCh38
NC_000007.13:g.107419780C= , CM000669.1:g.107419780C=	GRCh37
NC_000007.12:g.107207016C=	NCBI36
NG_008046.1:g.28899G= , LRG_683:g.28899G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340010.10:c.1407+333G= MANE Select	ENSP00000345873.5:n.1407+333G=
ENST00000340010.9:c.1407+333G=	ENSP00000345873.5:n.1407+333G=
ENST00000379083.7:c.*1198+333G=	ENSP00000368375.3:n.*1198+333G=
NM_000111.2:c.1407+333G= , LRG_683t1:c.1407+333G=	NP_000102.1:n.1407+333G=
XM_011515867.1:c.1407+333G=	XP_011514169.1:n.1407+333G=
NM_000111.3:c.1407+333G= MANE Select	NP_000102.1:n.1407+333G=