Canonical Allele Identifier: CA1105618626

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1791725497
• gnomAD v3: 7-107695862-T-TA
• gnomAD v4: 7-107695862-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695863dup , CM000669.2:g.107695863dup	GRCh38
NC_000007.13:g.107336308dup , CM000669.1:g.107336308dup	GRCh37
NC_000007.12:g.107123544dup	NCBI36
NG_008489.1:g.40229dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1438-70dup MANE Select	ENSP00000494017.1:n.1438-70dup
ENST00000644846.1:c.149-70dup
ENST00000265715.7:c.1438-70dup	ENSP00000265715.3:n.1438-70dup
ENST00000460748.1:n.541-70dup
ENST00000477350.5:n.285-70dup
ENST00000480841.5:n.287-70dup
ENST00000497446.5:n.453-70dup
NM_000441.1:c.1438-70dup	NP_000432.1:n.1438-70dup
XM_005250425.1:c.1438-70dup	XP_005250482.1:n.1438-70dup
XM_005250425.2:c.1438-70dup	XP_005250482.1:n.1438-70dup
XM_017012318.1:c.1360-70dup	XP_016867807.1:n.1360-70dup
NM_000441.2:c.1438-70dup MANE Select	NP_000432.1:n.1438-70dup