Canonical Allele Identifier: CA1732753009

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1791727080

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695903_107695905del , CM000669.2:g.107695903_107695905del	GRCh38
NC_000007.13:g.107336348_107336350del , CM000669.1:g.107336348_107336350del	GRCh37
NC_000007.12:g.107123584_107123586del	NCBI36
NG_008489.1:g.40269_40271del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1438-30_1438-28del MANE Select	ENSP00000494017.1:n.1438-30_1438-28del
ENST00000644846.1:c.149-30_149-28del
ENST00000265715.7:c.1438-30_1438-28del	ENSP00000265715.3:n.1438-30_1438-28del
ENST00000460748.1:n.541-30_541-28del
ENST00000477350.5:n.285-30_285-28del
ENST00000480841.5:n.287-30_287-28del
ENST00000497446.5:n.453-30_453-28del
NM_000441.1:c.1438-30_1438-28del	NP_000432.1:n.1438-30_1438-28del
XM_005250425.1:c.1438-30_1438-28del	XP_005250482.1:n.1438-30_1438-28del
XM_005250425.2:c.1438-30_1438-28del	XP_005250482.1:n.1438-30_1438-28del
XM_017012318.1:c.1360-30_1360-28del	XP_016867807.1:n.1360-30_1360-28del
NM_000441.2:c.1438-30_1438-28del MANE Select	NP_000432.1:n.1438-30_1438-28del