Canonical Allele Identifier: CA1590738388
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149980471T= , CM000667.2:g.149980471T= GRCh38
NC_000005.9:g.149360034T= , CM000667.1:g.149360034T= GRCh37
NC_000005.8:g.149340227T= NCBI36
NG_007147.2:g.21589T= , LRG_684:g.21589T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.878T= MANE Select ENSP00000286298.4:p.Val293=
ENST00000286298.4:c.878T= ENSP00000286298.4:p.Val293=
ENST00000503336.1:c.372+2120T= ENSP00000426053.1:n.372+2120T=
NM_000112.3:c.878T= , LRG_684t1:c.878T= NP_000103.2:p.Val293=
XM_017009191.2:c.878T= XP_016864680.1:p.Val293=
NM_000112.4:c.878T= MANE Select NP_000103.2:p.Val293=