Canonical Allele Identifier: CA2715574435
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs2129318223
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701806_107701807insCA , CM000669.2:g.107701806_107701807insCA GRCh38
NC_000007.13:g.107342251_107342252insCA , CM000669.1:g.107342251_107342252insCA GRCh37
NC_000007.12:g.107129487_107129488insCA NCBI36
NG_008489.1:g.46172_46173insCA

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1804-21_1804-20insCA MANE Select ENSP00000494017.1:n.1804-21_1804-20insCA
ENST00000644846.1:c.515-21_515-20insCA
ENST00000265715.7:c.1804-21_1804-20insCA ENSP00000265715.3:n.1804-21_1804-20insCA
ENST00000480841.5:n.653-21_653-20insCA
ENST00000492030.2:n.91-21_91-20insCA
NM_000441.1:c.1804-21_1804-20insCA NP_000432.1:n.1804-21_1804-20insCA
XM_005250425.1:c.1804-21_1804-20insCA XP_005250482.1:n.1804-21_1804-20insCA
XM_005250425.2:c.1804-21_1804-20insCA XP_005250482.1:n.1804-21_1804-20insCA
XM_017012318.1:c.1726-21_1726-20insCA XP_016867807.1:n.1726-21_1726-20insCA
NM_000441.2:c.1804-21_1804-20insCA MANE Select NP_000432.1:n.1804-21_1804-20insCA
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