Canonical Allele Identifier: CA577198929

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1316911906
• gnomAD v2: 7-107334789-A-T
• gnomAD v3: 7-107694344-A-T
• gnomAD v4: 7-107694344-A-T
• MyVariant Identifiers: chr7:g.107334789A>T (hg19) ; chr7:g.107694344A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694344A>T , CM000669.2:g.107694344A>T	GRCh38
NC_000007.13:g.107334789A>T , CM000669.1:g.107334789A>T	GRCh37
NC_000007.12:g.107122025A>T	NCBI36
NG_008489.1:g.38710A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1264-59A>T MANE Select	ENSP00000494017.1:n.1264-59A>T
ENST00000265715.7:c.1264-59A>T	ENSP00000265715.3:n.1264-59A>T
ENST00000460748.1:n.367-59A>T
ENST00000477350.5:n.189-277A>T
ENST00000480841.5:n.113-59A>T
ENST00000497446.5:n.279-59A>T
NM_000441.1:c.1264-59A>T	NP_000432.1:n.1264-59A>T
XM_005250425.1:c.1264-59A>T	XP_005250482.1:n.1264-59A>T
XM_006716025.2:c.*784A>T	XP_006716088.1:n.*784A>T
XM_005250425.2:c.1264-59A>T	XP_005250482.1:n.1264-59A>T
XM_006716025.3:c.*784A>T	XP_006716088.1:n.*784A>T
XM_017012318.1:c.1264-277A>T	XP_016867807.1:n.1264-277A>T
NM_000441.2:c.1264-59A>T MANE Select	NP_000432.1:n.1264-59A>T