Canonical Allele Identifier: CA1519346849
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144689_185144691delinsCCT , CM000666.2:g.185144689_185144691delinsCCT GRCh38
NC_000004.11:g.186065843_186065845delinsCCT , CM000666.1:g.186065843_186065845delinsCCT GRCh37
NC_000004.10:g.186302837_186302839delinsCCT NCBI36
NG_013001.1:g.6427_6429delinsCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-75_112-73delinsCCT MANE Select ENSP00000281456.5:n.112-75_112-73delinsCCT
ENST00000281456.10:c.112-75_112-73delinsCCT ENSP00000281456.5:n.112-75_112-73delinsCCT
ENST00000491736.1:c.112-75_112-73delinsCCT ENSP00000476711.1:n.112-75_112-73delinsCCT
NM_001151.3:c.112-75_112-73delinsCCT NP_001142.2:n.112-75_112-73delinsCCT
NM_001151.4:c.112-75_112-73delinsCCT MANE Select NP_001142.2:n.112-75_112-73delinsCCT