Canonical Allele Identifier: CA164214190

Gene: SLC26A4

Linked Data

• dbSNP Id: rs913104946
• MyVariant Identifiers: chr7:g.107334706T>A (hg19) ; chr7:g.107694261T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694261T>A , CM000669.2:g.107694261T>A	GRCh38
NC_000007.13:g.107334706T>A , CM000669.1:g.107334706T>A	GRCh37
NC_000007.12:g.107121942T>A	NCBI36
NG_008489.1:g.38627T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1264-142T>A MANE Select	ENSP00000494017.1:n.1264-142T>A
ENST00000265715.7:c.1264-142T>A	ENSP00000265715.3:n.1264-142T>A
ENST00000460748.1:n.367-142T>A
ENST00000477350.5:n.189-360T>A
ENST00000480841.5:n.113-142T>A
ENST00000497446.5:n.279-142T>A
NM_000441.1:c.1264-142T>A	NP_000432.1:n.1264-142T>A
XM_005250425.1:c.1264-142T>A	XP_005250482.1:n.1264-142T>A
XM_006716025.2:c.*701T>A	XP_006716088.1:n.*701T>A
XM_005250425.2:c.1264-142T>A	XP_005250482.1:n.1264-142T>A
XM_006716025.3:c.*701T>A	XP_006716088.1:n.*701T>A
XM_017012318.1:c.1264-360T>A	XP_016867807.1:n.1264-360T>A
NM_000441.2:c.1264-142T>A MANE Select	NP_000432.1:n.1264-142T>A