Canonical Allele Identifier: CA1732757150
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717410G= , CM000669.2:g.107717410G= GRCh38
NC_000007.13:g.107357855G= , CM000669.1:g.107357855G= GRCh37
NC_000007.12:g.107145091G= NCBI36
NG_008489.1:g.61776G=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1964G= MANE Select ENSP00000494017.1:n.*1964G=
ENST00000265715.7:c.*1964G= ENSP00000265715.3:n.*1964G=
NM_000441.1:c.*1964G= NP_000432.1:n.*1964G=
NM_000441.2:c.*1964G= MANE Select NP_000432.1:n.*1964G=
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