Canonical Allele Identifier: CA1519347036
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144816T= , CM000666.2:g.185144816T= GRCh38
NC_000004.11:g.186065970T= , CM000666.1:g.186065970T= GRCh37
NC_000004.10:g.186302964T= NCBI36
NG_013001.1:g.6554T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.164T= MANE Select ENSP00000281456.5:p.Ile55=
ENST00000281456.10:c.164T= ENSP00000281456.5:p.Ile55=
ENST00000491736.1:c.164T= ENSP00000476711.1:p.Ile55=
NM_001151.3:c.164T= NP_001142.2:p.Ile55=
NM_001151.4:c.164T= MANE Select NP_001142.2:p.Ile55=