Canonical Allele Identifier: CA831178018
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1400188364
MyVariant Identifiers: chr7:g.107329481del (hg19) chr7:g.107689036del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689036del , CM000669.2:g.107689036del GRCh38
NC_000007.13:g.107329481del , CM000669.1:g.107329481del GRCh37
NC_000007.12:g.107116717del NCBI36
NG_008489.1:g.33402del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1002-17del MANE Select ENSP00000494017.1:n.1002-17del
ENST00000265715.7:c.1002-17del ENSP00000265715.3:n.1002-17del
NM_000441.1:c.1002-17del NP_000432.1:n.1002-17del
XM_005250425.1:c.1002-17del XP_005250482.1:n.1002-17del
XM_006716025.2:c.1002-17del XP_006716088.1:n.1002-17del
XM_005250425.2:c.1002-17del XP_005250482.1:n.1002-17del
XM_006716025.3:c.1002-17del XP_006716088.1:n.1002-17del
XM_017012318.1:c.1002-17del XP_016867807.1:n.1002-17del
NM_000441.2:c.1002-17del MANE Select NP_000432.1:n.1002-17del
Search 100 bp 5'
Search 100 bp 3'