Canonical Allele Identifier: CA2684468716
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107710167-T-TGA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710167_107710168insGA , CM000669.2:g.107710167_107710168insGA GRCh38
NC_000007.13:g.107350612_107350613insGA , CM000669.1:g.107350612_107350613insGA GRCh37
NC_000007.12:g.107137848_107137849insGA NCBI36
NG_008489.1:g.54533_54534insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2203_2204insGA MANE Select ENSP00000494017.1:p.Ser735Ter
ENST00000644846.1:c.859_860insGA
ENST00000265715.7:c.2203_2204insGA ENSP00000265715.3:p.Ser735Ter
ENST00000492030.2:n.389_390insGA
NM_000441.1:c.2203_2204insGA NP_000432.1:p.Ser735Ter
XM_005250425.1:c.2203_2204insGA XP_005250482.1:p.Ser735Ter
XM_005250425.2:c.2203_2204insGA XP_005250482.1:p.Ser735Ter
XM_017012318.1:c.2125_2126insGA XP_016867807.1:p.Ser709Ter
NM_000441.2:c.2203_2204insGA MANE Select NP_000432.1:p.Ser735Ter
Search 100 bp 5'
Search 100 bp 3'