Canonical Allele Identifier: CA2684468964
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107701704-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701706del , CM000669.2:g.107701706del GRCh38
NC_000007.13:g.107342151del , CM000669.1:g.107342151del GRCh37
NC_000007.12:g.107129387del NCBI36
NG_008489.1:g.46072del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1804-121del MANE Select ENSP00000494017.1:n.1804-121del
ENST00000644846.1:c.515-121del
ENST00000265715.7:c.1804-121del ENSP00000265715.3:n.1804-121del
ENST00000480841.5:n.653-121del
ENST00000492030.2:n.91-121del
NM_000441.1:c.1804-121del NP_000432.1:n.1804-121del
XM_005250425.1:c.1804-121del XP_005250482.1:n.1804-121del
XM_005250425.2:c.1804-121del XP_005250482.1:n.1804-121del
XM_017012318.1:c.1726-121del XP_016867807.1:n.1726-121del
NM_000441.2:c.1804-121del MANE Select NP_000432.1:n.1804-121del
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