Canonical Allele Identifier: CA1590738387
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149980470G= , CM000667.2:g.149980470G= GRCh38
NC_000005.9:g.149360033G= , CM000667.1:g.149360033G= GRCh37
NC_000005.8:g.149340226G= NCBI36
NG_007147.2:g.21588G= , LRG_684:g.21588G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.877G= MANE Select ENSP00000286298.4:p.Val293=
ENST00000286298.4:c.877G= ENSP00000286298.4:p.Val293=
ENST00000503336.1:c.372+2119G= ENSP00000426053.1:n.372+2119G=
NM_000112.3:c.877G= , LRG_684t1:c.877G= NP_000103.2:p.Val293=
XM_017009191.2:c.877G= XP_016864680.1:p.Val293=
NM_000112.4:c.877G= MANE Select NP_000103.2:p.Val293=