Canonical Allele Identifier: CA1519346964
Gene: SLC25A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144751T= , CM000666.2:g.185144751T= GRCh38
NC_000004.11:g.186065905T= , CM000666.1:g.186065905T= GRCh37
NC_000004.10:g.186302899T= NCBI36
NG_013001.1:g.6489T=

Transcript Alleles

HGVS Amino-acid change
ENST00000281456.11:c.112-13T= MANE Select ENSP00000281456.5:n.112-13T=
ENST00000281456.10:c.112-13T= ENSP00000281456.5:n.112-13T=
ENST00000491736.1:c.112-13T= ENSP00000476711.1:n.112-13T=
NM_001151.3:c.112-13T= NP_001142.2:n.112-13T=
NM_001151.4:c.112-13T= MANE Select NP_001142.2:n.112-13T=
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