Canonical Allele Identifier: CA2684466516
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107690117T>G , CM000669.2:g.107690117T>G GRCh38
NC_000007.13:g.107330562T>G , CM000669.1:g.107330562T>G GRCh37
NC_000007.12:g.107117798T>G NCBI36
NG_008489.1:g.34483T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1150-7T>G MANE Select ENSP00000494017.1:n.1150-7T>G
ENST00000265715.7:c.1150-7T>G ENSP00000265715.3:n.1150-7T>G
NM_000441.1:c.1150-7T>G NP_000432.1:n.1150-7T>G
XM_005250425.1:c.1150-7T>G XP_005250482.1:n.1150-7T>G
XM_006716025.2:c.1150-7T>G XP_006716088.1:n.1150-7T>G
XM_005250425.2:c.1150-7T>G XP_005250482.1:n.1150-7T>G
XM_006716025.3:c.1150-7T>G XP_006716088.1:n.1150-7T>G
XM_017012318.1:c.1150-7T>G XP_016867807.1:n.1150-7T>G
NM_000441.2:c.1150-7T>G MANE Select NP_000432.1:n.1150-7T>G
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