Canonical Allele Identifier: CA358896341
Gene: SLC25A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144956G>C , CM000666.2:g.185144956G>C GRCh38
NC_000004.11:g.186066110G>C , CM000666.1:g.186066110G>C GRCh37
NC_000004.10:g.186303104G>C NCBI36
NG_013001.1:g.6694G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.304G>C MANE Select ENSP00000281456.5:p.Gly102Arg
ENST00000281456.10:c.304G>C ENSP00000281456.5:p.Gly102Arg
ENST00000491736.1:c.304G>C ENSP00000476711.1:p.Gly102Arg
NM_001151.3:c.304G>C NP_001142.2:p.Gly102Arg
NM_001151.4:c.304G>C MANE Select NP_001142.2:p.Gly102Arg