Canonical Allele Identifier: CA2546709244
Gene: SLC26A4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107716013_107716022del , CM000669.2:g.107716013_107716022del GRCh38
NC_000007.13:g.107356458_107356467del , CM000669.1:g.107356458_107356467del GRCh37
NC_000007.12:g.107143694_107143703del NCBI36
NG_008489.1:g.60379_60388del

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*567_*576del MANE Select ENSP00000494017.1:n.*567_*576del
ENST00000644846.1:c.1566_1575del
ENST00000265715.7:c.*567_*576del ENSP00000265715.3:n.*567_*576del
NM_000441.1:c.*567_*576del NP_000432.1:n.*567_*576del
XM_005250425.2:c.*567_*576del XP_005250482.1:n.*567_*576del
XM_017012318.1:c.*567_*576del XP_016867807.1:n.*567_*576del
NM_000441.2:c.*567_*576del MANE Select NP_000432.1:n.*567_*576del
Search 100 bp 5'
Search 100 bp 3'