Canonical Allele Identifier: CA1590739024

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149981959T= , CM000667.2:g.149981959T=	GRCh38
NC_000005.9:g.149361522T= , CM000667.1:g.149361522T=	GRCh37
NC_000005.8:g.149341715T=	NCBI36
NG_007147.2:g.23077T= , LRG_684:g.23077T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.*146T= MANE Select	ENSP00000286298.4:n.*146T=
ENST00000286298.4:c.*146T=	ENSP00000286298.4:n.*146T=
ENST00000503336.1:c.372+3608T=	ENSP00000426053.1:n.372+3608T=
NM_000112.3:c.*146T= , LRG_684t1:c.*146T=	NP_000103.2:n.*146T=
XM_017009191.2:c.*43T=	XP_016864680.1:n.*43T=
NM_000112.4:c.*146T= MANE Select	NP_000103.2:n.*146T=