Canonical Allele Identifier: CA368841361
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107696026C>G , CM000669.2:g.107696026C>G GRCh38
NC_000007.13:g.107336471C>G , CM000669.1:g.107336471C>G GRCh37
NC_000007.12:g.107123707C>G NCBI36
NG_008489.1:g.40392C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1531C>G MANE Select ENSP00000494017.1:p.Leu511Val
ENST00000644846.1:c.242C>G
ENST00000265715.7:c.1531C>G ENSP00000265715.3:p.Leu511Val
ENST00000477350.5:n.378C>G
ENST00000480841.5:n.380C>G
ENST00000497446.5:n.546C>G
NM_000441.1:c.1531C>G NP_000432.1:p.Leu511Val
XM_005250425.1:c.1531C>G XP_005250482.1:p.Leu511Val
XM_005250425.2:c.1531C>G XP_005250482.1:p.Leu511Val
XM_017012318.1:c.1453C>G XP_016867807.1:p.Leu485Val
NM_000441.2:c.1531C>G MANE Select NP_000432.1:p.Leu511Val