Canonical Allele Identifier: CA2684467607
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107694484-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107694486del , CM000669.2:g.107694486del GRCh38
NC_000007.13:g.107334931del , CM000669.1:g.107334931del GRCh37
NC_000007.12:g.107122167del NCBI36
NG_008489.1:g.38852del

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1341+6del MANE Select ENSP00000494017.1:n.1341+6del
ENST00000644846.1:c.52+6del
ENST00000265715.7:c.1341+6del ENSP00000265715.3:n.1341+6del
ENST00000460748.1:n.444+6del
ENST00000477350.5:n.189-135del
ENST00000480841.5:n.190+6del
ENST00000497446.5:n.356+6del
NM_000441.1:c.1341+6del NP_000432.1:n.1341+6del
XM_005250425.1:c.1341+6del XP_005250482.1:n.1341+6del
XM_005250425.2:c.1341+6del XP_005250482.1:n.1341+6del
XM_017012318.1:c.1264-135del XP_016867807.1:n.1264-135del
NM_000441.2:c.1341+6del MANE Select NP_000432.1:n.1341+6del
Search 100 bp 5'
Search 100 bp 3'