Canonical Allele Identifier: CA358895871
Gene: SLC25A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143478C>G , CM000666.2:g.185143478C>G GRCh38
NC_000004.11:g.186064632C>G , CM000666.1:g.186064632C>G GRCh37
NC_000004.10:g.186301626C>G NCBI36
NG_013001.1:g.5216C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.106C>G MANE Select ENSP00000281456.5:p.Leu36Val
ENST00000281456.10:c.106C>G ENSP00000281456.5:p.Leu36Val
ENST00000491736.1:c.106C>G ENSP00000476711.1:p.Leu36Val
NM_001151.3:c.106C>G NP_001142.2:p.Leu36Val
NM_001151.4:c.106C>G MANE Select NP_001142.2:p.Leu36Val