Canonical Allele Identifier: CA2684466222
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107683625-A-ATTTCACTGATACTCCTTCAATAGTCCTATTTG
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107683627_107683658dup , CM000669.2:g.107683627_107683658dup GRCh38
NC_000007.13:g.107324072_107324103dup , CM000669.1:g.107324072_107324103dup GRCh37
NC_000007.12:g.107111308_107111339dup NCBI36
NG_008489.1:g.27993_28024dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1001+90_1001+121dup MANE Select ENSP00000494017.1:n.1001+90_1001+121dup
ENST00000265715.7:c.1001+90_1001+121dup ENSP00000265715.3:n.1001+90_1001+121dup
NM_000441.1:c.1001+90_1001+121dup NP_000432.1:n.1001+90_1001+121dup
XM_005250425.1:c.1001+90_1001+121dup XP_005250482.1:n.1001+90_1001+121dup
XM_006716025.2:c.1001+90_1001+121dup XP_006716088.1:n.1001+90_1001+121dup
XM_005250425.2:c.1001+90_1001+121dup XP_005250482.1:n.1001+90_1001+121dup
XM_006716025.3:c.1001+90_1001+121dup XP_006716088.1:n.1001+90_1001+121dup
XM_017012318.1:c.1001+90_1001+121dup XP_016867807.1:n.1001+90_1001+121dup
NM_000441.2:c.1001+90_1001+121dup MANE Select NP_000432.1:n.1001+90_1001+121dup
Search 100 bp 5'
Search 100 bp 3'