Canonical Allele Identifier: CA1732757208
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717495A= , CM000669.2:g.107717495A= GRCh38
NC_000007.13:g.107357940A= , CM000669.1:g.107357940A= GRCh37
NC_000007.12:g.107145176A= NCBI36
NG_008489.1:g.61861A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.*2049A= MANE Select ENSP00000494017.1:n.*2049A=
ENST00000265715.7:c.*2049A= ENSP00000265715.3:n.*2049A=
NM_000441.1:c.*2049A= NP_000432.1:n.*2049A=
NM_000441.2:c.*2049A= MANE Select NP_000432.1:n.*2049A=
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