Canonical Allele Identifier: CA577029993
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1354259875

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695888C>T , CM000669.2:g.107695888C>T GRCh38
NC_000007.13:g.107336333C>T , CM000669.1:g.107336333C>T GRCh37
NC_000007.12:g.107123569C>T NCBI36
NG_008489.1:g.40254C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1438-45C>T MANE Select ENSP00000494017.1:n.1438-45C>T
ENST00000644846.1:c.149-45C>T
ENST00000265715.7:c.1438-45C>T ENSP00000265715.3:n.1438-45C>T
ENST00000460748.1:n.541-45C>T
ENST00000477350.5:n.285-45C>T
ENST00000480841.5:n.287-45C>T
ENST00000497446.5:n.453-45C>T
NM_000441.1:c.1438-45C>T NP_000432.1:n.1438-45C>T
XM_005250425.1:c.1438-45C>T XP_005250482.1:n.1438-45C>T
XM_005250425.2:c.1438-45C>T XP_005250482.1:n.1438-45C>T
XM_017012318.1:c.1360-45C>T XP_016867807.1:n.1360-45C>T
NM_000441.2:c.1438-45C>T MANE Select NP_000432.1:n.1438-45C>T