Canonical Allele Identifier: CA2684468528
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107709986-C-CT
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107709987dup , CM000669.2:g.107709987dup GRCh38
NC_000007.13:g.107350432dup , CM000669.1:g.107350432dup GRCh37
NC_000007.12:g.107137668dup NCBI36
NG_008489.1:g.54353dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2090-67dup MANE Select ENSP00000494017.1:n.2090-67dup
ENST00000644846.1:c.746-67dup
ENST00000265715.7:c.2090-67dup ENSP00000265715.3:n.2090-67dup
ENST00000492030.2:n.377-168dup
NM_000441.1:c.2090-67dup NP_000432.1:n.2090-67dup
XM_005250425.1:c.2090-67dup XP_005250482.1:n.2090-67dup
XM_005250425.2:c.2090-67dup XP_005250482.1:n.2090-67dup
XM_017012318.1:c.2012-67dup XP_016867807.1:n.2012-67dup
NM_000441.2:c.2090-67dup MANE Select NP_000432.1:n.2090-67dup
Search 100 bp 5'
Search 100 bp 3'