Canonical Allele Identifier: CA1732752978
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1791725899

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695870G>C , CM000669.2:g.107695870G>C GRCh38
NC_000007.13:g.107336315G>C , CM000669.1:g.107336315G>C GRCh37
NC_000007.12:g.107123551G>C NCBI36
NG_008489.1:g.40236G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1438-63G>C MANE Select ENSP00000494017.1:n.1438-63G>C
ENST00000644846.1:c.149-63G>C
ENST00000265715.7:c.1438-63G>C ENSP00000265715.3:n.1438-63G>C
ENST00000460748.1:n.541-63G>C
ENST00000477350.5:n.285-63G>C
ENST00000480841.5:n.287-63G>C
ENST00000497446.5:n.453-63G>C
NM_000441.1:c.1438-63G>C NP_000432.1:n.1438-63G>C
XM_005250425.1:c.1438-63G>C XP_005250482.1:n.1438-63G>C
XM_005250425.2:c.1438-63G>C XP_005250482.1:n.1438-63G>C
XM_017012318.1:c.1360-63G>C XP_016867807.1:n.1360-63G>C
NM_000441.2:c.1438-63G>C MANE Select NP_000432.1:n.1438-63G>C