Canonical Allele Identifier: CA1732755782
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1584349989
gnomAD v4: 7-107715999-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107715999T>A , CM000669.2:g.107715999T>A GRCh38
NC_000007.13:g.107356444T>A , CM000669.1:g.107356444T>A GRCh37
NC_000007.12:g.107143680T>A NCBI36
NG_008489.1:g.60365T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*553T>A MANE Select ENSP00000494017.1:n.*553T>A
ENST00000644846.1:c.1552T>A
ENST00000265715.7:c.*553T>A ENSP00000265715.3:n.*553T>A
NM_000441.1:c.*553T>A NP_000432.1:n.*553T>A
XM_005250425.2:c.*553T>A XP_005250482.1:n.*553T>A
XM_017012318.1:c.*553T>A XP_016867807.1:n.*553T>A
NM_000441.2:c.*553T>A MANE Select NP_000432.1:n.*553T>A
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