Canonical Allele Identifier: CA1590737367

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978025C= , CM000667.2:g.149978025C=	GRCh38
NC_000005.9:g.149357588C= , CM000667.1:g.149357588C=	GRCh37
NC_000005.8:g.149337781C=	NCBI36
NG_007147.2:g.19143C= , LRG_684:g.19143C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.605C=
ENST00000286298.5:c.373C= MANE Select	ENSP00000286298.4:p.Gln125=
ENST00000286298.4:c.373C=	ENSP00000286298.4:p.Gln125=
ENST00000503336.1:c.46C=	ENSP00000426053.1:p.Gln16=
NM_000112.3:c.373C= , LRG_684t1:c.373C=	NP_000103.2:p.Gln125=
XM_017009191.2:c.373C=	XP_016864680.1:p.Gln125=
NM_000112.4:c.373C= MANE Select	NP_000103.2:p.Gln125=