Canonical Allele Identifier: CA442615061
Gene: SLC25A4 HGNC NCBI

Linked Data

gnomAD v4: 4-185143477-G-T
MyVariant Identifiers: chr4:g.186064631G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143477G>T , CM000666.2:g.185143477G>T GRCh38
NC_000004.11:g.186064631G>T , CM000666.1:g.186064631G>T GRCh37
NC_000004.10:g.186301625G>T NCBI36
NG_013001.1:g.5215G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.105G>T MANE Select ENSP00000281456.5:p.Leu35=
ENST00000281456.10:c.105G>T ENSP00000281456.5:p.Leu35=
ENST00000491736.1:c.105G>T ENSP00000476711.1:p.Leu35=
NM_001151.3:c.105G>T NP_001142.2:p.Leu35=
NM_001151.4:c.105G>T MANE Select NP_001142.2:p.Leu35=
Search 100 bp 5'
Search 100 bp 3'