Canonical Allele Identifier: CA358895990
Gene: SLC25A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144803T>G , CM000666.2:g.185144803T>G GRCh38
NC_000004.11:g.186065957T>G , CM000666.1:g.186065957T>G GRCh37
NC_000004.10:g.186302951T>G NCBI36
NG_013001.1:g.6541T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.151T>G MANE Select ENSP00000281456.5:p.Tyr51Asp
ENST00000281456.10:c.151T>G ENSP00000281456.5:p.Tyr51Asp
ENST00000491736.1:c.151T>G ENSP00000476711.1:p.Tyr51Asp
NM_001151.3:c.151T>G NP_001142.2:p.Tyr51Asp
NM_001151.4:c.151T>G MANE Select NP_001142.2:p.Tyr51Asp