Canonical Allele Identifier: CA1590739010
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981938C= , CM000667.2:g.149981938C= GRCh38
NC_000005.9:g.149361501C= , CM000667.1:g.149361501C= GRCh37
NC_000005.8:g.149341694C= NCBI36
NG_007147.2:g.23056C= , LRG_684:g.23056C=

Transcript Alleles

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