Canonical Allele Identifier: CA1732759212
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701924_107701926delinsTAG , CM000669.2:g.107701924_107701926delinsTAG GRCh38
NC_000007.13:g.107342369_107342371delinsTAG , CM000669.1:g.107342369_107342371delinsTAG GRCh37
NC_000007.12:g.107129605_107129607delinsTAG NCBI36
NG_008489.1:g.46290_46292delinsTAG

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1901_1903delinsTAG MANE Select ENSP00000494017.1:p.Ile634=
ENST00000644846.1:c.612_614delinsTAG
ENST00000265715.7:c.1901_1903delinsTAG ENSP00000265715.3:p.Ile634=
ENST00000492030.2:n.188_190delinsTAG
NM_000441.1:c.1901_1903delinsTAG NP_000432.1:p.Ile634=
XM_005250425.1:c.1901_1903delinsTAG XP_005250482.1:p.Ile634=
XM_005250425.2:c.1901_1903delinsTAG XP_005250482.1:p.Ile634=
XM_017012318.1:c.1823_1825delinsTAG XP_016867807.1:p.Ile608=
NM_000441.2:c.1901_1903delinsTAG MANE Select NP_000432.1:p.Ile634=
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