Canonical Allele Identifier: CA368845509

Gene: SLC26A4

Linked Data

• ClinVar Variation Id: 810172
• ClinVar RCV Id: RCV000998890
• dbSNP Id: rs1584294942
• MyVariant Identifiers: chr7:g.107303823T>G (hg19) ; chr7:g.107663378T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107663378T>G , CM000669.2:g.107663378T>G	GRCh38
NC_000007.13:g.107303823T>G , CM000669.1:g.107303823T>G	GRCh37
NC_000007.12:g.107091059T>G	NCBI36
NG_008489.1:g.7744T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.247T>G MANE Select	ENSP00000494017.1:p.Trp83Gly
ENST00000265715.7:c.247T>G	ENSP00000265715.3:p.Trp83Gly
ENST00000440056.1:c.247T>G	ENSP00000394760.1:p.Trp83Gly
NM_000441.1:c.247T>G	NP_000432.1:p.Trp83Gly
XM_005250425.1:c.247T>G	XP_005250482.1:p.Trp83Gly
XM_006716025.2:c.247T>G	XP_006716088.1:p.Trp83Gly
XM_005250425.2:c.247T>G	XP_005250482.1:p.Trp83Gly
XM_006716025.3:c.247T>G	XP_006716088.1:p.Trp83Gly
XM_017012318.1:c.247T>G	XP_016867807.1:p.Trp83Gly
NM_000441.2:c.247T>G MANE Select	NP_000432.1:p.Trp83Gly