Canonical Allele Identifier: CA1519347379
Gene: SLC25A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185145042T= , CM000666.2:g.185145042T= GRCh38
NC_000004.11:g.186066196T= , CM000666.1:g.186066196T= GRCh37
NC_000004.10:g.186303190T= NCBI36
NG_013001.1:g.6780T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.390T= MANE Select ENSP00000281456.5:p.Phe130=
ENST00000281456.10:c.390T= ENSP00000281456.5:p.Phe130=
ENST00000491736.1:c.390T= ENSP00000476711.1:p.Phe130=
NM_001151.3:c.390T= NP_001142.2:p.Phe130=
NM_001151.4:c.390T= MANE Select NP_001142.2:p.Phe130=
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