Canonical Allele Identifier: CA1590737388

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978064G= , CM000667.2:g.149978064G=	GRCh38
NC_000005.9:g.149357627G= , CM000667.1:g.149357627G=	GRCh37
NC_000005.8:g.149337820G=	NCBI36
NG_007147.2:g.19182G= , LRG_684:g.19182G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.644G=
ENST00000286298.5:c.412G= MANE Select	ENSP00000286298.4:p.Val138=
ENST00000286298.4:c.412G=	ENSP00000286298.4:p.Val138=
ENST00000503336.1:c.85G=	ENSP00000426053.1:p.Val29=
NM_000112.3:c.412G= , LRG_684t1:c.412G=	NP_000103.2:p.Val138=
XM_017009191.2:c.412G=	XP_016864680.1:p.Val138=
NM_000112.4:c.412G= MANE Select	NP_000103.2:p.Val138=