Canonical Allele Identifier: CA1732755771
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1792336348
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107715983T>C , CM000669.2:g.107715983T>C GRCh38
NC_000007.13:g.107356428T>C , CM000669.1:g.107356428T>C GRCh37
NC_000007.12:g.107143664T>C NCBI36
NG_008489.1:g.60349T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*537T>C MANE Select ENSP00000494017.1:n.*537T>C
ENST00000644846.1:c.1536T>C
ENST00000265715.7:c.*537T>C ENSP00000265715.3:n.*537T>C
NM_000441.1:c.*537T>C NP_000432.1:n.*537T>C
XM_005250425.2:c.*537T>C XP_005250482.1:n.*537T>C
XM_017012318.1:c.*537T>C XP_016867807.1:n.*537T>C
NM_000441.2:c.*537T>C MANE Select NP_000432.1:n.*537T>C
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