Canonical Allele Identifier: CA358895690
Gene: SLC25A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143392G>C , CM000666.2:g.185143392G>C GRCh38
NC_000004.11:g.186064546G>C , CM000666.1:g.186064546G>C GRCh37
NC_000004.10:g.186301540G>C NCBI36
NG_013001.1:g.5130G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.20G>C MANE Select ENSP00000281456.5:p.Ser7Thr
ENST00000281456.10:c.20G>C ENSP00000281456.5:p.Ser7Thr
ENST00000491736.1:c.20G>C ENSP00000476711.1:p.Ser7Thr
NM_001151.3:c.20G>C NP_001142.2:p.Ser7Thr
NM_001151.4:c.20G>C MANE Select NP_001142.2:p.Ser7Thr