Canonical Allele Identifier: CA1590738997
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981899G= , CM000667.2:g.149981899G= GRCh38
NC_000005.9:g.149361462G= , CM000667.1:g.149361462G= GRCh37
NC_000005.8:g.149341655G= NCBI36
NG_007147.2:g.23017G= , LRG_684:g.23017G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*86G= MANE Select ENSP00000286298.4:n.*86G=
ENST00000286298.4:c.*86G= ENSP00000286298.4:n.*86G=
ENST00000503336.1:c.372+3548G= ENSP00000426053.1:n.372+3548G=
NM_000112.3:c.*86G= , LRG_684t1:c.*86G= NP_000103.2:n.*86G=
XM_017009191.2:c.*13-30G= XP_016864680.1:n.*13-30G=
NM_000112.4:c.*86G= MANE Select NP_000103.2:n.*86G=