Canonical Allele Identifier: CA358896440
Gene: SLC25A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185145002T>A , CM000666.2:g.185145002T>A GRCh38
NC_000004.11:g.186066156T>A , CM000666.1:g.186066156T>A GRCh37
NC_000004.10:g.186303150T>A NCBI36
NG_013001.1:g.6740T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.350T>A MANE Select ENSP00000281456.5:p.Leu117Gln
ENST00000281456.10:c.350T>A ENSP00000281456.5:p.Leu117Gln
ENST00000491736.1:c.350T>A ENSP00000476711.1:p.Leu117Gln
NM_001151.3:c.350T>A NP_001142.2:p.Leu117Gln
NM_001151.4:c.350T>A MANE Select NP_001142.2:p.Leu117Gln