Canonical Allele Identifier: CA1519345538
Gene: SLC25A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143396C= , CM000666.2:g.185143396C= GRCh38
NC_000004.11:g.186064550C= , CM000666.1:g.186064550C= GRCh37
NC_000004.10:g.186301544C= NCBI36
NG_013001.1:g.5134C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.24C= MANE Select ENSP00000281456.5:p.Phe8=
ENST00000281456.10:c.24C= ENSP00000281456.5:p.Phe8=
ENST00000491736.1:c.24C= ENSP00000476711.1:p.Phe8=
NM_001151.3:c.24C= NP_001142.2:p.Phe8=
NM_001151.4:c.24C= MANE Select NP_001142.2:p.Phe8=
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