Canonical Allele Identifier: CA358896451
Gene: SLC25A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185145008C>G , CM000666.2:g.185145008C>G GRCh38
NC_000004.11:g.186066162C>G , CM000666.1:g.186066162C>G GRCh37
NC_000004.10:g.186303156C>G NCBI36
NG_013001.1:g.6746C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.356C>G MANE Select ENSP00000281456.5:p.Ser119Cys
ENST00000281456.10:c.356C>G ENSP00000281456.5:p.Ser119Cys
ENST00000491736.1:c.356C>G ENSP00000476711.1:p.Ser119Cys
NM_001151.3:c.356C>G NP_001142.2:p.Ser119Cys
NM_001151.4:c.356C>G MANE Select NP_001142.2:p.Ser119Cys