Canonical Allele Identifier: CA2675943486
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978379_149978382del , CM000667.2:g.149978379_149978382del GRCh38
NC_000005.9:g.149357942_149357945del , CM000667.1:g.149357942_149357945del GRCh37
NC_000005.8:g.149338135_149338138del NCBI36
NG_007147.2:g.19497_19500del , LRG_684:g.19497_19500del

Transcript Alleles

HGVS Amino-acid change
ENST00000690410.1:n.959_962del
ENST00000286298.5:c.699+28_699+31del MANE Select ENSP00000286298.4:n.699+28_699+31del
ENST00000286298.4:c.699+28_699+31del ENSP00000286298.4:n.699+28_699+31del
ENST00000503336.1:c.372+28_372+31del ENSP00000426053.1:n.372+28_372+31del
NM_000112.3:c.699+28_699+31del , LRG_684t1:c.699+28_699+31del NP_000103.2:n.699+28_699+31del
XM_017009191.2:c.699+28_699+31del XP_016864680.1:n.699+28_699+31del
NM_000112.4:c.699+28_699+31del MANE Select NP_000103.2:n.699+28_699+31del