Canonical Allele Identifier: CA2684469535
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107715990_107715994del , CM000669.2:g.107715990_107715994del GRCh38
NC_000007.13:g.107356435_107356439del , CM000669.1:g.107356435_107356439del GRCh37
NC_000007.12:g.107143671_107143675del NCBI36
NG_008489.1:g.60356_60360del

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*544_*548del MANE Select ENSP00000494017.1:n.*544_*548del
ENST00000644846.1:c.1543_1547del
ENST00000265715.7:c.*544_*548del ENSP00000265715.3:n.*544_*548del
NM_000441.1:c.*544_*548del NP_000432.1:n.*544_*548del
XM_005250425.2:c.*544_*548del XP_005250482.1:n.*544_*548del
XM_017012318.1:c.*544_*548del XP_016867807.1:n.*544_*548del
NM_000441.2:c.*544_*548del MANE Select NP_000432.1:n.*544_*548del