Canonical Allele Identifier: CA447401997

Gene: SLC26A2

Linked Data

• MyVariant Identifiers: chr5:g.149357665T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978102T>A , CM000667.2:g.149978102T>A	GRCh38
NC_000005.9:g.149357665T>A , CM000667.1:g.149357665T>A	GRCh37
NC_000005.8:g.149337858T>A	NCBI36
NG_007147.2:g.19220T>A , LRG_684:g.19220T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.682T>A
ENST00000286298.5:c.450T>A MANE Select	ENSP00000286298.4:p.Ile150=
ENST00000286298.4:c.450T>A	ENSP00000286298.4:p.Ile150=
ENST00000503336.1:c.123T>A	ENSP00000426053.1:p.Ile41=
NM_000112.3:c.450T>A , LRG_684t1:c.450T>A	NP_000103.2:p.Ile150=
XM_017009191.2:c.450T>A	XP_016864680.1:p.Ile150=
NM_000112.4:c.450T>A MANE Select	NP_000103.2:p.Ile150=