Canonical Allele Identifier: CA358896181
Gene: SLC25A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144887A>T , CM000666.2:g.185144887A>T GRCh38
NC_000004.11:g.186066041A>T , CM000666.1:g.186066041A>T GRCh37
NC_000004.10:g.186303035A>T NCBI36
NG_013001.1:g.6625A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000281456.11:c.235A>T MANE Select ENSP00000281456.5:p.Ile79Phe
ENST00000281456.10:c.235A>T ENSP00000281456.5:p.Ile79Phe
ENST00000491736.1:c.235A>T ENSP00000476711.1:p.Ile79Phe
NM_001151.3:c.235A>T NP_001142.2:p.Ile79Phe
NM_001151.4:c.235A>T MANE Select NP_001142.2:p.Ile79Phe