Canonical Allele Identifier: CA358896346
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1734411377

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144959G>A , CM000666.2:g.185144959G>A GRCh38
NC_000004.11:g.186066113G>A , CM000666.1:g.186066113G>A GRCh37
NC_000004.10:g.186303107G>A NCBI36
NG_013001.1:g.6697G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.307G>A MANE Select ENSP00000281456.5:p.Val103Met
ENST00000281456.10:c.307G>A ENSP00000281456.5:p.Val103Met
ENST00000491736.1:c.307G>A ENSP00000476711.1:p.Val103Met
NM_001151.3:c.307G>A NP_001142.2:p.Val103Met
NM_001151.4:c.307G>A MANE Select NP_001142.2:p.Val103Met