Canonical Allele Identifier: CA1590738688
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981217_149981243delinsGTCATCCTCCGCACTCAGAAGCCAAAG , CM000667.2:g.149981217_149981243delinsGTCATCCTCCGCACTCAGAAGCCAAAG GRCh38
NC_000005.9:g.149360780_149360806delinsGTCATCCTCCGCACTCAGAAGCCAAAG , CM000667.1:g.149360780_149360806delinsGTCATCCTCCGCACTCAGAAGCCAAAG GRCh37
NC_000005.8:g.149340973_149340999delinsGTCATCCTCCGCACTCAGAAGCCAAAG NCBI36
NG_007147.2:g.22335_22361delinsGTCATCCTCCGCACTCAGAAGCCAAAG , LRG_684:g.22335_22361delinsGTCATCCTCCGCACTCAGAAGCCAAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000286298.5:c.1624_1650delinsGTCATCCTCCGCACTCAGAAGCCAAAG MANE Select ENSP00000286298.4:p.Val542=
ENST00000286298.4:c.1624_1650delinsGTCATCCTCCGCACTCAGAAGCCAAAG ENSP00000286298.4:p.Val542=
ENST00000503336.1:c.372+2866_372+2892delinsGTCATCCTCCGCACTCAGAAGCCAAAG ENSP00000426053.1:n.372+2866_372+2892delinsGTCATCCTCCGCACTCAG...
NM_000112.3:c.1624_1650delinsGTCATCCTCCGCACTCAGAAGCCAAAG , LRG_684t1:c.1624_1650delinsGTCATCCTCCGCACTCAGAAGCCAAAG NP_000103.2:p.Val542=
XM_017009191.2:c.1624_1650delinsGTCATCCTCCGCACTCAGAAGCCAAAG XP_016864680.1:p.Val542=
NM_000112.4:c.1624_1650delinsGTCATCCTCCGCACTCAGAAGCCAAAG MANE Select NP_000103.2:p.Val542=