Canonical Allele Identifier: CA2507418979
Gene: SLC26A2 HGNC NCBI

Linked Data

gnomAD v4: 5-149981878-A-ACT
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981878_149981879insCT , CM000667.2:g.149981878_149981879insCT GRCh38
NC_000005.9:g.149361441_149361442insCT , CM000667.1:g.149361441_149361442insCT GRCh37
NC_000005.8:g.149341634_149341635insCT NCBI36
NG_007147.2:g.22996_22997insCT , LRG_684:g.22996_22997insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*65_*66insCT MANE Select ENSP00000286298.4:n.*65_*66insCT
ENST00000286298.4:c.*65_*66insCT ENSP00000286298.4:n.*65_*66insCT
ENST00000503336.1:c.372+3527_372+3528insCT ENSP00000426053.1:n.372+3527_372+3528insCT
NM_000112.3:c.*65_*66insCT , LRG_684t1:c.*65_*66insCT NP_000103.2:n.*65_*66insCT
XM_017009191.2:c.*13-51_*13-50insCT XP_016864680.1:n.*13-51_*13-50insCT
NM_000112.4:c.*65_*66insCT MANE Select NP_000103.2:n.*65_*66insCT
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