Canonical Allele Identifier: CA1519347200
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144953G= , CM000666.2:g.185144953G= GRCh38
NC_000004.11:g.186066107G= , CM000666.1:g.186066107G= GRCh37
NC_000004.10:g.186303101G= NCBI36
NG_013001.1:g.6691G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.301G= MANE Select ENSP00000281456.5:p.Gly101=
ENST00000281456.10:c.301G= ENSP00000281456.5:p.Gly101=
ENST00000491736.1:c.301G= ENSP00000476711.1:p.Gly101=
NM_001151.3:c.301G= NP_001142.2:p.Gly101=
NM_001151.4:c.301G= MANE Select NP_001142.2:p.Gly101=