Canonical Allele Identifier: CA358895897
Gene: SLC25A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.186065919T>A (hg19) chr4:g.185144765T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144765T>A , CM000666.2:g.185144765T>A GRCh38
NC_000004.11:g.186065919T>A , CM000666.1:g.186065919T>A GRCh37
NC_000004.10:g.186302913T>A NCBI36
NG_013001.1:g.6503T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.113T>A MANE Select ENSP00000281456.5:p.Val38Asp
ENST00000281456.10:c.113T>A ENSP00000281456.5:p.Val38Asp
ENST00000491736.1:c.113T>A ENSP00000476711.1:p.Val38Asp
NM_001151.3:c.113T>A NP_001142.2:p.Val38Asp
NM_001151.4:c.113T>A MANE Select NP_001142.2:p.Val38Asp
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