Canonical Allele Identifier: CA1590738760
Gene: SLC26A2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981398_149981402delinsAAACT , CM000667.2:g.149981398_149981402delinsAAACT GRCh38
NC_000005.9:g.149360961_149360965delinsAAACT , CM000667.1:g.149360961_149360965delinsAAACT GRCh37
NC_000005.8:g.149341154_149341158delinsAAACT NCBI36
NG_007147.2:g.22516_22520delinsAAACT , LRG_684:g.22516_22520delinsAAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.1805_1809delinsAAACT MANE Select ENSP00000286298.4:p.Gln602=
ENST00000286298.4:c.1805_1809delinsAAACT ENSP00000286298.4:p.Gln602=
ENST00000503336.1:c.372+3047_372+3051delinsAAACT ENSP00000426053.1:n.372+3047_372+3051delinsAAACT
NM_000112.3:c.1805_1809delinsAAACT , LRG_684t1:c.1805_1809delinsAAACT NP_000103.2:p.Gln602=
XM_017009191.2:c.1805_1809delinsAAACT XP_016864680.1:p.Gln602=
NM_000112.4:c.1805_1809delinsAAACT MANE Select NP_000103.2:p.Gln602=
Search 100 bp 5'
Search 100 bp 3'