Canonical Allele Identifier: CA10625018
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 358504
dbSNP Id: rs727503432

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107715419A>G , CM000669.2:g.107715419A>G GRCh38
NC_000007.13:g.107355864A>G , CM000669.1:g.107355864A>G GRCh37
NC_000007.12:g.107143100A>G NCBI36
NG_008489.1:g.59785A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.2320-4A>G MANE Select ENSP00000494017.1:n.2320-4A>G
ENST00000644846.1:c.976-4A>G
ENST00000265715.7:c.2320-4A>G ENSP00000265715.3:n.2320-4A>G
ENST00000492030.2:n.506-4A>G
NM_000441.1:c.2320-4A>G NP_000432.1:n.2320-4A>G
XM_005250425.1:c.2320-4A>G XP_005250482.1:n.2320-4A>G
XM_005250425.2:c.2320-4A>G XP_005250482.1:n.2320-4A>G
XM_017012318.1:c.2242-4A>G XP_016867807.1:n.2242-4A>G
NM_000441.2:c.2320-4A>G MANE Select NP_000432.1:n.2320-4A>G