Canonical Allele Identifier: CA442615039
Gene: SLC25A4 HGNC NCBI

Linked Data

gnomAD v4: 4-185143474-G-T
MyVariant Identifiers: chr4:g.186064628G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143474G>T , CM000666.2:g.185143474G>T GRCh38
NC_000004.11:g.186064628G>T , CM000666.1:g.186064628G>T GRCh37
NC_000004.10:g.186301622G>T NCBI36
NG_013001.1:g.5212G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.102G>T MANE Select ENSP00000281456.5:p.Leu34=
ENST00000281456.10:c.102G>T ENSP00000281456.5:p.Leu34=
ENST00000491736.1:c.102G>T ENSP00000476711.1:p.Leu34=
NM_001151.3:c.102G>T NP_001142.2:p.Leu34=
NM_001151.4:c.102G>T MANE Select NP_001142.2:p.Leu34=
Search 100 bp 5'
Search 100 bp 3'