Canonical Allele Identifier: CA368845864

Gene: SLC26A4

Linked Data

• dbSNP Id: rs746238617
• gnomAD v2: 7-107303882-T-A
• gnomAD v3: 7-107663437-T-A
• gnomAD v4: 7-107663437-T-A
• MyVariant Identifiers: chr7:g.107303882T>A (hg19) ; chr7:g.107663437T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107663437T>A , CM000669.2:g.107663437T>A	GRCh38
NC_000007.13:g.107303882T>A , CM000669.1:g.107303882T>A	GRCh37
NC_000007.12:g.107091118T>A	NCBI36
NG_008489.1:g.7803T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.304+2T>A MANE Select	ENSP00000494017.1:n.304+2T>A
ENST00000265715.7:c.304+2T>A	ENSP00000265715.3:n.304+2T>A
ENST00000440056.1:c.304+2T>A	ENSP00000394760.1:n.304+2T>A
NM_000441.1:c.304+2T>A	NP_000432.1:n.304+2T>A
XM_005250425.1:c.304+2T>A	XP_005250482.1:n.304+2T>A
XM_006716025.2:c.304+2T>A	XP_006716088.1:n.304+2T>A
XM_005250425.2:c.304+2T>A	XP_005250482.1:n.304+2T>A
XM_006716025.3:c.304+2T>A	XP_006716088.1:n.304+2T>A
XM_017012318.1:c.304+2T>A	XP_016867807.1:n.304+2T>A
NM_000441.2:c.304+2T>A MANE Select	NP_000432.1:n.304+2T>A