Canonical Allele Identifier: CA1732753459
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107696181G= , CM000669.2:g.107696181G= GRCh38
NC_000007.13:g.107336626G= , CM000669.1:g.107336626G= GRCh37
NC_000007.12:g.107123862G= NCBI36
NG_008489.1:g.40547G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1544+142G= MANE Select ENSP00000494017.1:n.1544+142G=
ENST00000644846.1:c.255+142G=
ENST00000265715.7:c.1544+142G= ENSP00000265715.3:n.1544+142G=
ENST00000477350.5:n.391+142G=
ENST00000480841.5:n.393+142G=
NM_000441.1:c.1544+142G= NP_000432.1:n.1544+142G=
XM_005250425.1:c.1544+142G= XP_005250482.1:n.1544+142G=
XM_005250425.2:c.1544+142G= XP_005250482.1:n.1544+142G=
XM_017012318.1:c.1466+142G= XP_016867807.1:n.1466+142G=
NM_000441.2:c.1544+142G= MANE Select NP_000432.1:n.1544+142G=
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