Canonical Allele Identifier: CA1732757148
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717406T= , CM000669.2:g.107717406T= GRCh38
NC_000007.13:g.107357851T= , CM000669.1:g.107357851T= GRCh37
NC_000007.12:g.107145087T= NCBI36
NG_008489.1:g.61772T=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1960T= MANE Select ENSP00000494017.1:n.*1960T=
ENST00000265715.7:c.*1960T= ENSP00000265715.3:n.*1960T=
NM_000441.1:c.*1960T= NP_000432.1:n.*1960T=
NM_000441.2:c.*1960T= MANE Select NP_000432.1:n.*1960T=
Search 100 bp 5'
Search 100 bp 3'