Canonical Allele Identifier: CA1732756981
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717324C= , CM000669.2:g.107717324C= GRCh38
NC_000007.13:g.107357769C= , CM000669.1:g.107357769C= GRCh37
NC_000007.12:g.107145005C= NCBI36
NG_008489.1:g.61690C=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1878C= MANE Select ENSP00000494017.1:n.*1878C=
ENST00000644846.1:c.2877C=
ENST00000265715.7:c.*1878C= ENSP00000265715.3:n.*1878C=
NM_000441.1:c.*1878C= NP_000432.1:n.*1878C=
NM_000441.2:c.*1878C= MANE Select NP_000432.1:n.*1878C=
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