Canonical Allele Identifier: CA4432816
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs748042149

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695902T>A , CM000669.2:g.107695902T>A GRCh38
NC_000007.13:g.107336347T>A , CM000669.1:g.107336347T>A GRCh37
NC_000007.12:g.107123583T>A NCBI36
NG_008489.1:g.40268T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1438-31T>A MANE Select ENSP00000494017.1:n.1438-31T>A
ENST00000644846.1:c.149-31T>A
ENST00000265715.7:c.1438-31T>A ENSP00000265715.3:n.1438-31T>A
ENST00000460748.1:n.541-31T>A
ENST00000477350.5:n.285-31T>A
ENST00000480841.5:n.287-31T>A
ENST00000497446.5:n.453-31T>A
NM_000441.1:c.1438-31T>A NP_000432.1:n.1438-31T>A
XM_005250425.1:c.1438-31T>A XP_005250482.1:n.1438-31T>A
XM_005250425.2:c.1438-31T>A XP_005250482.1:n.1438-31T>A
XM_017012318.1:c.1360-31T>A XP_016867807.1:n.1360-31T>A
NM_000441.2:c.1438-31T>A MANE Select NP_000432.1:n.1438-31T>A