Canonical Allele Identifier: CA1732748724

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1791536106

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107690417_107690419del , CM000669.2:g.107690417_107690419del	GRCh38
NC_000007.13:g.107330862_107330864del , CM000669.1:g.107330862_107330864del	GRCh37
NC_000007.12:g.107118098_107118100del	NCBI36
NG_008489.1:g.34783_34785del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1263+180_1263+182del MANE Select	ENSP00000494017.1:n.1263+180_1263+182del
ENST00000265715.7:c.1263+180_1263+182del	ENSP00000265715.3:n.1263+180_1263+182del
NM_000441.1:c.1263+180_1263+182del	NP_000432.1:n.1263+180_1263+182del
XM_005250425.1:c.1263+180_1263+182del	XP_005250482.1:n.1263+180_1263+182del
XM_006716025.2:c.1263+180_1263+182del	XP_006716088.1:n.1263+180_1263+182del
XM_005250425.2:c.1263+180_1263+182del	XP_005250482.1:n.1263+180_1263+182del
XM_006716025.3:c.1263+180_1263+182del	XP_006716088.1:n.1263+180_1263+182del
XM_017012318.1:c.1263+180_1263+182del	XP_016867807.1:n.1263+180_1263+182del
NM_000441.2:c.1263+180_1263+182del MANE Select	NP_000432.1:n.1263+180_1263+182del