Canonical Allele Identifier: CA1732752983
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1791726113

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695876A>G , CM000669.2:g.107695876A>G GRCh38
NC_000007.13:g.107336321A>G , CM000669.1:g.107336321A>G GRCh37
NC_000007.12:g.107123557A>G NCBI36
NG_008489.1:g.40242A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1438-57A>G MANE Select ENSP00000494017.1:n.1438-57A>G
ENST00000644846.1:c.149-57A>G
ENST00000265715.7:c.1438-57A>G ENSP00000265715.3:n.1438-57A>G
ENST00000460748.1:n.541-57A>G
ENST00000477350.5:n.285-57A>G
ENST00000480841.5:n.287-57A>G
ENST00000497446.5:n.453-57A>G
NM_000441.1:c.1438-57A>G NP_000432.1:n.1438-57A>G
XM_005250425.1:c.1438-57A>G XP_005250482.1:n.1438-57A>G
XM_005250425.2:c.1438-57A>G XP_005250482.1:n.1438-57A>G
XM_017012318.1:c.1360-57A>G XP_016867807.1:n.1360-57A>G
NM_000441.2:c.1438-57A>G MANE Select NP_000432.1:n.1438-57A>G