Canonical Allele Identifier: CA577198837

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1297751022
• gnomAD v2: 7-107302485-T-TG
• gnomAD v3: 7-107662040-T-TG
• gnomAD v4: 7-107662040-T-TG
• MyVariant Identifiers: chr7:g.107302485_107302486insG (hg19) ; chr7:g.107662040_107662041insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107662044dup , CM000669.2:g.107662044dup	GRCh38
NC_000007.13:g.107302489dup , CM000669.1:g.107302489dup	GRCh37
NC_000007.12:g.107089725dup	NCBI36
NG_008489.1:g.6410dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.164+239dup MANE Select	ENSP00000494017.1:n.164+239dup
ENST00000265715.7:c.164+239dup	ENSP00000265715.3:n.164+239dup
ENST00000440056.1:c.164+239dup	ENSP00000394760.1:n.164+239dup
NM_000441.1:c.164+239dup	NP_000432.1:n.164+239dup
XM_005250425.1:c.164+239dup	XP_005250482.1:n.164+239dup
XM_006716025.2:c.164+239dup	XP_006716088.1:n.164+239dup
XM_005250425.2:c.164+239dup	XP_005250482.1:n.164+239dup
XM_006716025.3:c.164+239dup	XP_006716088.1:n.164+239dup
XM_017012318.1:c.164+239dup	XP_016867807.1:n.164+239dup
NM_000441.2:c.164+239dup MANE Select	NP_000432.1:n.164+239dup