Canonical Allele Identifier: CA1732759058
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701800T= , CM000669.2:g.107701800T= GRCh38
NC_000007.13:g.107342245T= , CM000669.1:g.107342245T= GRCh37
NC_000007.12:g.107129481T= NCBI36
NG_008489.1:g.46166T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1804-27T= MANE Select ENSP00000494017.1:n.1804-27T=
ENST00000644846.1:c.515-27T=
ENST00000265715.7:c.1804-27T= ENSP00000265715.3:n.1804-27T=
ENST00000480841.5:n.653-27T=
ENST00000492030.2:n.91-27T=
NM_000441.1:c.1804-27T= NP_000432.1:n.1804-27T=
XM_005250425.1:c.1804-27T= XP_005250482.1:n.1804-27T=
XM_005250425.2:c.1804-27T= XP_005250482.1:n.1804-27T=
XM_017012318.1:c.1726-27T= XP_016867807.1:n.1726-27T=
NM_000441.2:c.1804-27T= MANE Select NP_000432.1:n.1804-27T=
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