Canonical Allele Identifier: CA831183757

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1386897076
• gnomAD v3: 7-107696379-G-GT
• gnomAD v4: 7-107696379-G-GT
• MyVariant Identifiers: chr7:g.107336824_107336825insT (hg19) ; chr7:g.107696379_107696380insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107696380dup , CM000669.2:g.107696380dup	GRCh38
NC_000007.13:g.107336825dup , CM000669.1:g.107336825dup	GRCh37
NC_000007.12:g.107124061dup	NCBI36
NG_008489.1:g.40746dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1544+341dup MANE Select	ENSP00000494017.1:n.1544+341dup
ENST00000644846.1:c.255+341dup
ENST00000265715.7:c.1544+341dup	ENSP00000265715.3:n.1544+341dup
ENST00000477350.5:n.391+341dup
ENST00000480841.5:n.393+341dup
NM_000441.1:c.1544+341dup	NP_000432.1:n.1544+341dup
XM_005250425.1:c.1544+341dup	XP_005250482.1:n.1544+341dup
XM_005250425.2:c.1544+341dup	XP_005250482.1:n.1544+341dup
XM_017012318.1:c.1466+341dup	XP_016867807.1:n.1466+341dup
NM_000441.2:c.1544+341dup MANE Select	NP_000432.1:n.1544+341dup