Canonical Allele Identifier: CA1519347265
Gene: SLC25A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144991T= , CM000666.2:g.185144991T= GRCh38
NC_000004.11:g.186066145T= , CM000666.1:g.186066145T= GRCh37
NC_000004.10:g.186303139T= NCBI36
NG_013001.1:g.6729T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.339T= MANE Select ENSP00000281456.5:p.Phe113=
ENST00000281456.10:c.339T= ENSP00000281456.5:p.Phe113=
ENST00000491736.1:c.339T= ENSP00000476711.1:p.Phe113=
NM_001151.3:c.339T= NP_001142.2:p.Phe113=
NM_001151.4:c.339T= MANE Select NP_001142.2:p.Phe113=
Search 100 bp 5'
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