Canonical Allele Identifier: CA1732787480

Gene: SLC26A3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107779672T= , CM000669.2:g.107779672T=	GRCh38
NC_000007.13:g.107420117T= , CM000669.1:g.107420117T=	GRCh37
NC_000007.12:g.107207353T=	NCBI36
NG_008046.1:g.28562A= , LRG_683:g.28562A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000340010.10:c.1403A= MANE Select	ENSP00000345873.5:p.Asp468=
ENST00000340010.9:c.1403A=	ENSP00000345873.5:p.Asp468=
ENST00000379083.7:c.*1194A=	ENSP00000368375.3:n.*1194A=
NM_000111.2:c.1403A= , LRG_683t1:c.1403A=	NP_000102.1:p.Asp468=
XM_011515867.1:c.1403A=	XP_011514169.1:p.Asp468=
NM_000111.3:c.1403A= MANE Select	NP_000102.1:p.Asp468=