Canonical Allele Identifier: CA1590738991
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981882C= , CM000667.2:g.149981882C= GRCh38
NC_000005.9:g.149361445C= , CM000667.1:g.149361445C= GRCh37
NC_000005.8:g.149341638C= NCBI36
NG_007147.2:g.23000C= , LRG_684:g.23000C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*69C= MANE Select ENSP00000286298.4:n.*69C=
ENST00000286298.4:c.*69C= ENSP00000286298.4:n.*69C=
ENST00000503336.1:c.372+3531C= ENSP00000426053.1:n.372+3531C=
NM_000112.3:c.*69C= , LRG_684t1:c.*69C= NP_000103.2:n.*69C=
XM_017009191.2:c.*13-47C= XP_016864680.1:n.*13-47C=
NM_000112.4:c.*69C= MANE Select NP_000103.2:n.*69C=