Canonical Allele Identifier: CA1590738548
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149980858G= , CM000667.2:g.149980858G= GRCh38
NC_000005.9:g.149360421G= , CM000667.1:g.149360421G= GRCh37
NC_000005.8:g.149340614G= NCBI36
NG_007147.2:g.21976G= , LRG_684:g.21976G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.1265G= MANE Select ENSP00000286298.4:p.Gly422=
ENST00000286298.4:c.1265G= ENSP00000286298.4:p.Gly422=
ENST00000503336.1:c.372+2507G= ENSP00000426053.1:n.372+2507G=
NM_000112.3:c.1265G= , LRG_684t1:c.1265G= NP_000103.2:p.Gly422=
XM_017009191.2:c.1265G= XP_016864680.1:p.Gly422=
NM_000112.4:c.1265G= MANE Select NP_000103.2:p.Gly422=