Canonical Allele Identifier: CA577029892
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1327096914

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695854C>T , CM000669.2:g.107695854C>T GRCh38
NC_000007.13:g.107336299C>T , CM000669.1:g.107336299C>T GRCh37
NC_000007.12:g.107123535C>T NCBI36
NG_008489.1:g.40220C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1438-79C>T MANE Select ENSP00000494017.1:n.1438-79C>T
ENST00000644846.1:c.149-79C>T
ENST00000265715.7:c.1438-79C>T ENSP00000265715.3:n.1438-79C>T
ENST00000460748.1:n.541-79C>T
ENST00000477350.5:n.285-79C>T
ENST00000480841.5:n.287-79C>T
ENST00000497446.5:n.453-79C>T
NM_000441.1:c.1438-79C>T NP_000432.1:n.1438-79C>T
XM_005250425.1:c.1438-79C>T XP_005250482.1:n.1438-79C>T
XM_005250425.2:c.1438-79C>T XP_005250482.1:n.1438-79C>T
XM_017012318.1:c.1360-79C>T XP_016867807.1:n.1360-79C>T
NM_000441.2:c.1438-79C>T MANE Select NP_000432.1:n.1438-79C>T