Canonical Allele Identifier: CA577198940

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1484644471
• gnomAD v2: 7-107334939-T-A
• gnomAD v4: 7-107694494-T-A
• MyVariant Identifiers: chr7:g.107334939T>A (hg19) ; chr7:g.107694494T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694494T>A , CM000669.2:g.107694494T>A	GRCh38
NC_000007.13:g.107334939T>A , CM000669.1:g.107334939T>A	GRCh37
NC_000007.12:g.107122175T>A	NCBI36
NG_008489.1:g.38860T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1341+14T>A MANE Select	ENSP00000494017.1:n.1341+14T>A
ENST00000644846.1:c.52+14T>A
ENST00000265715.7:c.1341+14T>A	ENSP00000265715.3:n.1341+14T>A
ENST00000460748.1:n.444+14T>A
ENST00000477350.5:n.189-127T>A
ENST00000480841.5:n.190+14T>A
ENST00000497446.5:n.356+14T>A
NM_000441.1:c.1341+14T>A	NP_000432.1:n.1341+14T>A
XM_005250425.1:c.1341+14T>A	XP_005250482.1:n.1341+14T>A
XM_005250425.2:c.1341+14T>A	XP_005250482.1:n.1341+14T>A
XM_017012318.1:c.1264-127T>A	XP_016867807.1:n.1264-127T>A
NM_000441.2:c.1341+14T>A MANE Select	NP_000432.1:n.1341+14T>A