Canonical Allele Identifier: CA2532009568
Gene: SLC26A4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107715965A>G , CM000669.2:g.107715965A>G GRCh38
NC_000007.13:g.107356410A>G , CM000669.1:g.107356410A>G GRCh37
NC_000007.12:g.107143646A>G NCBI36
NG_008489.1:g.60331A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*519A>G MANE Select ENSP00000494017.1:n.*519A>G
ENST00000644846.1:c.1518A>G
ENST00000265715.7:c.*519A>G ENSP00000265715.3:n.*519A>G
NM_000441.1:c.*519A>G NP_000432.1:n.*519A>G
XM_005250425.2:c.*519A>G XP_005250482.1:n.*519A>G
XM_017012318.1:c.*519A>G XP_016867807.1:n.*519A>G
NM_000441.2:c.*519A>G MANE Select NP_000432.1:n.*519A>G
Search 100 bp 5'
Search 100 bp 3'