Canonical Allele Identifier: CA16609564
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 402275
ClinVar RCV Id: RCV000454360
dbSNP Id: rs1060499807

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689201del , CM000669.2:g.107689201del GRCh38
NC_000007.13:g.107329646del , CM000669.1:g.107329646del GRCh37
NC_000007.12:g.107116882del NCBI36
NG_008489.1:g.33567del

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1149+1del
ENST00000265715.7:c.1149+1del
NM_000441.1:c.1149+1del
XM_005250425.1:c.1149+1del
XM_006716025.2:c.1149+1del
XM_005250425.2:c.1149+1del
XM_006716025.3:c.1149+1del
XM_017012318.1:c.1149+1del
NM_000441.2:c.1149+1del