Canonical Allele Identifier: CA2675943632
Gene: SLC26A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149980269_149980272del , CM000667.2:g.149980269_149980272del GRCh38
NC_000005.9:g.149359832_149359835del , CM000667.1:g.149359832_149359835del GRCh37
NC_000005.8:g.149340025_149340028del NCBI36
NG_007147.2:g.21387_21390del , LRG_684:g.21387_21390del

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.700-24_700-21del MANE Select ENSP00000286298.4:n.700-24_700-21del
ENST00000286298.4:c.700-24_700-21del ENSP00000286298.4:n.700-24_700-21del
ENST00000503336.1:c.372+1918_372+1921del ENSP00000426053.1:n.372+1918_372+1921del
NM_000112.3:c.700-24_700-21del , LRG_684t1:c.700-24_700-21del NP_000103.2:n.700-24_700-21del
XM_017009191.2:c.700-24_700-21del XP_016864680.1:n.700-24_700-21del
NM_000112.4:c.700-24_700-21del MANE Select NP_000103.2:n.700-24_700-21del