Canonical Allele Identifier: CA1590738933
Gene: SLC26A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981766_149981770delinsCAGAA , CM000667.2:g.149981766_149981770delinsCAGAA GRCh38
NC_000005.9:g.149361329_149361333delinsCAGAA , CM000667.1:g.149361329_149361333delinsCAGAA GRCh37
NC_000005.8:g.149341522_149341526delinsCAGAA NCBI36
NG_007147.2:g.22884_22888delinsCAGAA , LRG_684:g.22884_22888delinsCAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.2173_2177delinsCAGAA MANE Select ENSP00000286298.4:p.Gln725=
ENST00000286298.4:c.2173_2177delinsCAGAA ENSP00000286298.4:p.Gln725=
ENST00000503336.1:c.372+3415_372+3419delinsCAGAA ENSP00000426053.1:n.372+3415_372+3419delinsCAGAA
NM_000112.3:c.2173_2177delinsCAGAA , LRG_684t1:c.2173_2177delinsCAGAA NP_000103.2:p.Gln725=
XM_017009191.2:c.2173_2177delinsCAGAA XP_016864680.1:p.Gln725=
NM_000112.4:c.2173_2177delinsCAGAA MANE Select NP_000103.2:p.Gln725=
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