Canonical Allele Identifier: CA2684465555
Gene: SLC26A4 HGNC NCBI
SLC26A4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107661523_107661524insT , CM000669.2:g.107661523_107661524insT GRCh38
NC_000007.13:g.107301968_107301969insT , CM000669.1:g.107301968_107301969insT GRCh37
NC_000007.12:g.107089204_107089205insT NCBI36
NG_008489.1:g.5889_5890insT

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.-3-116_-3-115insT (SLC26A4) MANE Select ENSP00000494017.1:n.-3-116_-3-115insT
ENST00000265715.7:c.-3-116_-3-115insT (SLC26A4) ENSP00000265715.3:n.-3-116_-3-115insT
ENST00000440056.1:c.-3-116_-3-115insT (SLC26A4) ENSP00000394760.1:n.-3-116_-3-115insT
NM_000441.1:c.-3-116_-3-115insT (SLC26A4) NP_000432.1:n.-3-116_-3-115insT
NR_028137.1:n.197+78_197+79insA (SLC26A4-AS1)
XM_005250425.1:c.-3-116_-3-115insT (SLC26A4) XP_005250482.1:n.-3-116_-3-115insT
XM_005250425.2:c.-3-116_-3-115insT (SLC26A4) XP_005250482.1:n.-3-116_-3-115insT
NM_000441.2:c.-3-116_-3-115insT (SLC26A4) MANE Select NP_000432.1:n.-3-116_-3-115insT