Canonical Allele Identifier: CA1519345461
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143346G= , CM000666.2:g.185143346G= GRCh38
NC_000004.11:g.186064500G= , CM000666.1:g.186064500G= GRCh37
NC_000004.10:g.186301494G= NCBI36
NG_013001.1:g.5084G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.-27G= MANE Select ENSP00000281456.5:n.-27G=
ENST00000281456.10:c.-27G= ENSP00000281456.5:n.-27G=
ENST00000491736.1:c.-27G= ENSP00000476711.1:n.-27G=
NM_001151.3:c.-27G= NP_001142.2:n.-27G=
NM_001151.4:c.-27G= MANE Select NP_001142.2:n.-27G=