Canonical Allele Identifier: CA368839332
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107690233C>G , CM000669.2:g.107690233C>G GRCh38
NC_000007.13:g.107330678C>G , CM000669.1:g.107330678C>G GRCh37
NC_000007.12:g.107117914C>G NCBI36
NG_008489.1:g.34599C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1259C>G MANE Select ENSP00000494017.1:p.Thr420Arg
ENST00000265715.7:c.1259C>G ENSP00000265715.3:p.Thr420Arg
NM_000441.1:c.1259C>G NP_000432.1:p.Thr420Arg
XM_005250425.1:c.1259C>G XP_005250482.1:p.Thr420Arg
XM_006716025.2:c.1259C>G XP_006716088.1:p.Thr420Arg
XM_005250425.2:c.1259C>G XP_005250482.1:p.Thr420Arg
XM_006716025.3:c.1259C>G XP_006716088.1:p.Thr420Arg
XM_017012318.1:c.1259C>G XP_016867807.1:p.Thr420Arg
NM_000441.2:c.1259C>G MANE Select NP_000432.1:p.Thr420Arg