Canonical Allele Identifier: CA4433068
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 756195
dbSNP Id: rs758851434

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710149C>T , CM000669.2:g.107710149C>T GRCh38
NC_000007.13:g.107350594C>T , CM000669.1:g.107350594C>T GRCh37
NC_000007.12:g.107137830C>T NCBI36
NG_008489.1:g.54515C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2185C>T MANE Select ENSP00000494017.1:p.Leu729=
ENST00000644846.1:c.841C>T
ENST00000265715.7:c.2185C>T ENSP00000265715.3:p.Leu729=
ENST00000492030.2:n.377-6C>T
NM_000441.1:c.2185C>T NP_000432.1:p.Leu729=
XM_005250425.1:c.2185C>T XP_005250482.1:p.Leu729=
XM_005250425.2:c.2185C>T XP_005250482.1:p.Leu729=
XM_017012318.1:c.2107C>T XP_016867807.1:p.Leu703=
NM_000441.2:c.2185C>T MANE Select NP_000432.1:p.Leu729=