Canonical Allele Identifier: CA1732750971
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107709875A= , CM000669.2:g.107709875A= GRCh38
NC_000007.13:g.107350320A= , CM000669.1:g.107350320A= GRCh37
NC_000007.12:g.107137556A= NCBI36
NG_008489.1:g.54241A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2090-179A= MANE Select ENSP00000494017.1:n.2090-179A=
ENST00000644846.1:c.746-179A=
ENST00000265715.7:c.2090-179A= ENSP00000265715.3:n.2090-179A=
ENST00000492030.2:n.377-280A=
NM_000441.1:c.2090-179A= NP_000432.1:n.2090-179A=
XM_005250425.1:c.2090-179A= XP_005250482.1:n.2090-179A=
XM_005250425.2:c.2090-179A= XP_005250482.1:n.2090-179A=
XM_017012318.1:c.2012-179A= XP_016867807.1:n.2012-179A=
NM_000441.2:c.2090-179A= MANE Select NP_000432.1:n.2090-179A=
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