Canonical Allele Identifier: CA2542741318

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107695817-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695827_107695828dup , CM000669.2:g.107695827_107695828dup	GRCh38
NC_000007.13:g.107336272_107336273dup , CM000669.1:g.107336272_107336273dup	GRCh37
NC_000007.12:g.107123508_107123509dup	NCBI36
NG_008489.1:g.40193_40194dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1438-106_1438-105dup MANE Select	ENSP00000494017.1:n.1438-106_1438-105dup
ENST00000644846.1:c.149-106_149-105dup
ENST00000265715.7:c.1438-106_1438-105dup	ENSP00000265715.3:n.1438-106_1438-105dup
ENST00000460748.1:n.541-106_541-105dup
ENST00000477350.5:n.285-106_285-105dup
ENST00000480841.5:n.287-106_287-105dup
ENST00000497446.5:n.453-106_453-105dup
NM_000441.1:c.1438-106_1438-105dup	NP_000432.1:n.1438-106_1438-105dup
XM_005250425.1:c.1438-106_1438-105dup	XP_005250482.1:n.1438-106_1438-105dup
XM_005250425.2:c.1438-106_1438-105dup	XP_005250482.1:n.1438-106_1438-105dup
XM_017012318.1:c.1360-106_1360-105dup	XP_016867807.1:n.1360-106_1360-105dup
NM_000441.2:c.1438-106_1438-105dup MANE Select	NP_000432.1:n.1438-106_1438-105dup