Canonical Allele Identifier: CA1590737437
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978174G= , CM000667.2:g.149978174G= GRCh38
NC_000005.9:g.149357737G= , CM000667.1:g.149357737G= GRCh37
NC_000005.8:g.149337930G= NCBI36
NG_007147.2:g.19292G= , LRG_684:g.19292G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.754G=
ENST00000286298.5:c.522G= MANE Select ENSP00000286298.4:p.Glu174=
ENST00000286298.4:c.522G= ENSP00000286298.4:p.Glu174=
ENST00000503336.1:c.195G= ENSP00000426053.1:p.Glu65=
NM_000112.3:c.522G= , LRG_684t1:c.522G= NP_000103.2:p.Glu174=
XM_017009191.2:c.522G= XP_016864680.1:p.Glu174=
NM_000112.4:c.522G= MANE Select NP_000103.2:p.Glu174=