Canonical Allele Identifier: CA2684467959
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107697946-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107697947del , CM000669.2:g.107697947del GRCh38
NC_000007.13:g.107338392del , CM000669.1:g.107338392del GRCh37
NC_000007.12:g.107125628del NCBI36
NG_008489.1:g.42313del

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1545-95del MANE Select ENSP00000494017.1:n.1545-95del
ENST00000644846.1:c.256-95del
ENST00000265715.7:c.1545-95del ENSP00000265715.3:n.1545-95del
ENST00000477350.5:n.392-95del
ENST00000480841.5:n.394-95del
NM_000441.1:c.1545-95del NP_000432.1:n.1545-95del
XM_005250425.1:c.1545-95del XP_005250482.1:n.1545-95del
XM_005250425.2:c.1545-95del XP_005250482.1:n.1545-95del
XM_017012318.1:c.1467-95del XP_016867807.1:n.1467-95del
NM_000441.2:c.1545-95del MANE Select NP_000432.1:n.1545-95del
Search 100 bp 5'
Search 100 bp 3'