Canonical Allele Identifier: CA2568861386
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981937_149981938insTAT , CM000667.2:g.149981937_149981938insTAT GRCh38
NC_000005.9:g.149361500_149361501insTAT , CM000667.1:g.149361500_149361501insTAT GRCh37
NC_000005.8:g.149341693_149341694insTAT NCBI36
NG_007147.2:g.23055_23056insTAT , LRG_684:g.23055_23056insTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*124_*125insTAT MANE Select ENSP00000286298.4:n.*124_*125insTAT
ENST00000286298.4:c.*124_*125insTAT ENSP00000286298.4:n.*124_*125insTAT
ENST00000503336.1:c.372+3586_372+3587insTAT ENSP00000426053.1:n.372+3586_372+3587insTAT
NM_000112.3:c.*124_*125insTAT , LRG_684t1:c.*124_*125insTAT NP_000103.2:n.*124_*125insTAT
XM_017009191.2:c.*21_*22insTAT XP_016864680.1:n.*21_*22insTAT
NM_000112.4:c.*124_*125insTAT MANE Select NP_000103.2:n.*124_*125insTAT