Canonical Allele Identifier: CA1519347050
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144826G= , CM000666.2:g.185144826G= GRCh38
NC_000004.11:g.186065980G= , CM000666.1:g.186065980G= GRCh37
NC_000004.10:g.186302974G= NCBI36
NG_013001.1:g.6564G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.174G= MANE Select ENSP00000281456.5:p.Val58=
ENST00000281456.10:c.174G= ENSP00000281456.5:p.Val58=
ENST00000491736.1:c.174G= ENSP00000476711.1:p.Val58=
NM_001151.3:c.174G= NP_001142.2:p.Val58=
NM_001151.4:c.174G= MANE Select NP_001142.2:p.Val58=