Canonical Allele Identifier: CA368840374
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107334899G>C (hg19) chr7:g.107694454G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107694454G>C , CM000669.2:g.107694454G>C GRCh38
NC_000007.13:g.107334899G>C , CM000669.1:g.107334899G>C GRCh37
NC_000007.12:g.107122135G>C NCBI36
NG_008489.1:g.38820G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1315G>C MANE Select ENSP00000494017.1:p.Gly439Arg
ENST00000644846.1:c.26G>C
ENST00000265715.7:c.1315G>C ENSP00000265715.3:p.Gly439Arg
ENST00000460748.1:n.418G>C
ENST00000477350.5:n.189-167G>C
ENST00000480841.5:n.164G>C
ENST00000497446.5:n.330G>C
NM_000441.1:c.1315G>C NP_000432.1:p.Gly439Arg
XM_005250425.1:c.1315G>C XP_005250482.1:p.Gly439Arg
XM_005250425.2:c.1315G>C XP_005250482.1:p.Gly439Arg
XM_017012318.1:c.1264-167G>C XP_016867807.1:n.1264-167G>C
NM_000441.2:c.1315G>C MANE Select NP_000432.1:p.Gly439Arg
Search 100 bp 5'
Search 100 bp 3'