Canonical Allele Identifier: CA1519346807
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144659T= , CM000666.2:g.185144659T= GRCh38
NC_000004.11:g.186065813T= , CM000666.1:g.186065813T= GRCh37
NC_000004.10:g.186302807T= NCBI36
NG_013001.1:g.6397T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-105T= MANE Select ENSP00000281456.5:n.112-105T=
ENST00000281456.10:c.112-105T= ENSP00000281456.5:n.112-105T=
ENST00000491736.1:c.112-105T= ENSP00000476711.1:n.112-105T=
NM_001151.3:c.112-105T= NP_001142.2:n.112-105T=
NM_001151.4:c.112-105T= MANE Select NP_001142.2:n.112-105T=