Canonical Allele Identifier: CA2558754573
Gene: SLC26A4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107683440T>C , CM000669.2:g.107683440T>C GRCh38
NC_000007.13:g.107323885T>C , CM000669.1:g.107323885T>C GRCh37
NC_000007.12:g.107111121T>C NCBI36
NG_008489.1:g.27806T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.919-15T>C MANE Select ENSP00000494017.1:n.919-15T>C
ENST00000265715.7:c.919-15T>C ENSP00000265715.3:n.919-15T>C
NM_000441.1:c.919-15T>C NP_000432.1:n.919-15T>C
XM_005250425.1:c.919-15T>C XP_005250482.1:n.919-15T>C
XM_006716025.2:c.919-15T>C XP_006716088.1:n.919-15T>C
XM_005250425.2:c.919-15T>C XP_005250482.1:n.919-15T>C
XM_006716025.3:c.919-15T>C XP_006716088.1:n.919-15T>C
XM_017012318.1:c.919-15T>C XP_016867807.1:n.919-15T>C
NM_000441.2:c.919-15T>C MANE Select NP_000432.1:n.919-15T>C
Search 100 bp 5'
Search 100 bp 3'