Canonical Allele Identifier: CA358895920
Gene: SLC25A4 HGNC NCBI

Linked Data

COSMIC: COSM5011374
MyVariant Identifiers: chr4:g.186065928C>T (hg19) chr4:g.185144774C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144774C>T , CM000666.2:g.185144774C>T GRCh38
NC_000004.11:g.186065928C>T , CM000666.1:g.186065928C>T GRCh37
NC_000004.10:g.186302922C>T NCBI36
NG_013001.1:g.6512C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.122C>T MANE Select ENSP00000281456.5:p.Ala41Val
ENST00000281456.10:c.122C>T ENSP00000281456.5:p.Ala41Val
ENST00000491736.1:c.122C>T ENSP00000476711.1:p.Ala41Val
NM_001151.3:c.122C>T NP_001142.2:p.Ala41Val
NM_001151.4:c.122C>T MANE Select NP_001142.2:p.Ala41Val
Search 100 bp 5'
Search 100 bp 3'