Canonical Allele Identifier: CA1519347100
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144880C= , CM000666.2:g.185144880C= GRCh38
NC_000004.11:g.186066034C= , CM000666.1:g.186066034C= GRCh37
NC_000004.10:g.186303028C= NCBI36
NG_013001.1:g.6618C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.228C= MANE Select ENSP00000281456.5:p.Ala76=
ENST00000281456.10:c.228C= ENSP00000281456.5:p.Ala76=
ENST00000491736.1:c.228C= ENSP00000476711.1:p.Ala76=
NM_001151.3:c.228C= NP_001142.2:p.Ala76=
NM_001151.4:c.228C= MANE Select NP_001142.2:p.Ala76=