Canonical Allele Identifier: CA358896109
Gene: SLC25A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144855T>A , CM000666.2:g.185144855T>A GRCh38
NC_000004.11:g.186066009T>A , CM000666.1:g.186066009T>A GRCh37
NC_000004.10:g.186303003T>A NCBI36
NG_013001.1:g.6593T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000281456.11:c.203T>A MANE Select ENSP00000281456.5:p.Leu68His
ENST00000281456.10:c.203T>A ENSP00000281456.5:p.Leu68His
ENST00000491736.1:c.203T>A ENSP00000476711.1:p.Leu68His
NM_001151.3:c.203T>A NP_001142.2:p.Leu68His
NM_001151.4:c.203T>A MANE Select NP_001142.2:p.Leu68His