Canonical Allele Identifier: CA1590739007
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981926T= , CM000667.2:g.149981926T= GRCh38
NC_000005.9:g.149361489T= , CM000667.1:g.149361489T= GRCh37
NC_000005.8:g.149341682T= NCBI36
NG_007147.2:g.23044T= , LRG_684:g.23044T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*113T= MANE Select ENSP00000286298.4:n.*113T=
ENST00000286298.4:c.*113T= ENSP00000286298.4:n.*113T=
ENST00000503336.1:c.372+3575T= ENSP00000426053.1:n.372+3575T=
NM_000112.3:c.*113T= , LRG_684t1:c.*113T= NP_000103.2:n.*113T=
XM_017009191.2:c.*13-3T= XP_016864680.1:n.*13-3T=
NM_000112.4:c.*113T= MANE Select NP_000103.2:n.*113T=