Canonical Allele Identifier: CA831193292
Gene: SLC26A3 HGNC NCBI

Linked Data

dbSNP Id: rs1218820222
MyVariant Identifiers: chr7:g.107408120del (hg19) chr7:g.107767675del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767678del , CM000669.2:g.107767678del GRCh38
NC_000007.13:g.107408123del , CM000669.1:g.107408123del GRCh37
NC_000007.12:g.107195359del NCBI36
NG_008046.1:g.40559del , LRG_683:g.40559del

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2206-31del MANE Select ENSP00000345873.5:n.2206-31del
ENST00000340010.9:c.2206-31del ENSP00000345873.5:n.2206-31del
ENST00000379083.7:c.*1763-31del ENSP00000368375.3:n.*1763-31del
NM_000111.2:c.2206-31del , LRG_683t1:c.2206-31del NP_000102.1:n.2206-31del
XM_011515867.1:c.2206-31del XP_011514169.1:n.2206-31del
NM_000111.3:c.2206-31del MANE Select NP_000102.1:n.2206-31del
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