Canonical Allele Identifier: CA1732757180
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717450T= , CM000669.2:g.107717450T= GRCh38
NC_000007.13:g.107357895T= , CM000669.1:g.107357895T= GRCh37
NC_000007.12:g.107145131T= NCBI36
NG_008489.1:g.61816T=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*2004T= MANE Select ENSP00000494017.1:n.*2004T=
ENST00000265715.7:c.*2004T= ENSP00000265715.3:n.*2004T=
NM_000441.1:c.*2004T= NP_000432.1:n.*2004T=
NM_000441.2:c.*2004T= MANE Select NP_000432.1:n.*2004T=
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