Canonical Allele Identifier: CA3505365

Gene: SLC26A2

Linked Data

• ClinVar Variation Id: 1084226
• ClinVar RCV Id: RCV001401197 ; RCV001831426
• dbSNP Id: rs376300575
• ExAC: 5:149360152 G / A
• gnomAD v2: 5-149360152-G-A
• gnomAD v3: 5-149980589-G-A
• gnomAD v4: 5-149980589-G-A
• COSMIC: COSM1064225
• MyVariant Identifiers: chr5:g.149360152G>A (hg19) ; chr5:g.149980589G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149980589G>A , CM000667.2:g.149980589G>A	GRCh38
NC_000005.9:g.149360152G>A , CM000667.1:g.149360152G>A	GRCh37
NC_000005.8:g.149340345G>A	NCBI36
NG_007147.2:g.21707G>A , LRG_684:g.21707G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286298.5:c.996G>A MANE Select	ENSP00000286298.4:p.Pro332=
ENST00000286298.4:c.996G>A	ENSP00000286298.4:p.Pro332=
ENST00000503336.1:c.372+2238G>A	ENSP00000426053.1:n.372+2238G>A
NM_000112.3:c.996G>A , LRG_684t1:c.996G>A	NP_000103.2:p.Pro332=
XM_017009191.2:c.996G>A	XP_016864680.1:p.Pro332=
NM_000112.4:c.996G>A MANE Select	NP_000103.2:p.Pro332=