Canonical Allele Identifier: CA1732757154
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717411C= , CM000669.2:g.107717411C= GRCh38
NC_000007.13:g.107357856C= , CM000669.1:g.107357856C= GRCh37
NC_000007.12:g.107145092C= NCBI36
NG_008489.1:g.61777C=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1965C= MANE Select ENSP00000494017.1:n.*1965C=
ENST00000265715.7:c.*1965C= ENSP00000265715.3:n.*1965C=
NM_000441.1:c.*1965C= NP_000432.1:n.*1965C=
NM_000441.2:c.*1965C= MANE Select NP_000432.1:n.*1965C=
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