Canonical Allele Identifier: CA2684465577
Gene: SLC26A4 HGNC NCBI
SLC26A4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107661529_107661530insC , CM000669.2:g.107661529_107661530insC GRCh38
NC_000007.13:g.107301974_107301975insC , CM000669.1:g.107301974_107301975insC GRCh37
NC_000007.12:g.107089210_107089211insC NCBI36
NG_008489.1:g.5895_5896insC

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.-3-110_-3-109insC (SLC26A4) MANE Select ENSP00000494017.1:n.-3-110_-3-109insC
ENST00000265715.7:c.-3-110_-3-109insC (SLC26A4) ENSP00000265715.3:n.-3-110_-3-109insC
ENST00000440056.1:c.-3-110_-3-109insC (SLC26A4) ENSP00000394760.1:n.-3-110_-3-109insC
NM_000441.1:c.-3-110_-3-109insC (SLC26A4) NP_000432.1:n.-3-110_-3-109insC
NR_028137.1:n.197+72_197+73insG (SLC26A4-AS1)
XM_005250425.1:c.-3-110_-3-109insC (SLC26A4) XP_005250482.1:n.-3-110_-3-109insC
XM_005250425.2:c.-3-110_-3-109insC (SLC26A4) XP_005250482.1:n.-3-110_-3-109insC
NM_000441.2:c.-3-110_-3-109insC (SLC26A4) MANE Select NP_000432.1:n.-3-110_-3-109insC