Canonical Allele Identifier: CA1590738383
Gene: SLC26A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149980466A= , CM000667.2:g.149980466A= GRCh38
NC_000005.9:g.149360029A= , CM000667.1:g.149360029A= GRCh37
NC_000005.8:g.149340222A= NCBI36
NG_007147.2:g.21584A= , LRG_684:g.21584A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.873A= MANE Select ENSP00000286298.4:p.Ile291=
ENST00000286298.4:c.873A= ENSP00000286298.4:p.Ile291=
ENST00000503336.1:c.372+2115A= ENSP00000426053.1:n.372+2115A=
NM_000112.3:c.873A= , LRG_684t1:c.873A= NP_000103.2:p.Ile291=
XM_017009191.2:c.873A= XP_016864680.1:p.Ile291=
NM_000112.4:c.873A= MANE Select NP_000103.2:p.Ile291=