Canonical Allele Identifier: CA2578449453
Gene: SLC26A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149980261del , CM000667.2:g.149980261del GRCh38
NC_000005.9:g.149359824del , CM000667.1:g.149359824del GRCh37
NC_000005.8:g.149340017del NCBI36
NG_007147.2:g.21379del , LRG_684:g.21379del

Transcript Alleles

HGVS Amino-acid change
ENST00000286298.5:c.700-32del MANE Select ENSP00000286298.4:n.700-32del
ENST00000286298.4:c.700-32del ENSP00000286298.4:n.700-32del
ENST00000503336.1:c.372+1910del ENSP00000426053.1:n.372+1910del
NM_000112.3:c.700-32del , LRG_684t1:c.700-32del NP_000103.2:n.700-32del
XM_017009191.2:c.700-32del XP_016864680.1:n.700-32del
NM_000112.4:c.700-32del MANE Select NP_000103.2:n.700-32del
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