Canonical Allele Identifier: CA2695198368

Gene: SLC26A4

Linked Data

• ClinVar Variation Id: 2678902
• ClinVar RCV Id: RCV003472878 ; RCV003689099

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107689053del , CM000669.2:g.107689053del	GRCh38
NC_000007.13:g.107329498del , CM000669.1:g.107329498del	GRCh37
NC_000007.12:g.107116734del	NCBI36
NG_008489.1:g.33419del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1002del
ENST00000265715.7:c.1002del
NM_000441.1:c.1002del
XM_005250425.1:c.1002del
XM_006716025.2:c.1002del
XM_005250425.2:c.1002del
XM_006716025.3:c.1002del
XM_017012318.1:c.1002del
NM_000441.2:c.1002del