Canonical Allele Identifier: CA1519345681
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143496C= , CM000666.2:g.185143496C= GRCh38
NC_000004.11:g.186064650C= , CM000666.1:g.186064650C= GRCh37
NC_000004.10:g.186301644C= NCBI36
NG_013001.1:g.5234C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.111+13C= MANE Select ENSP00000281456.5:n.111+13C=
ENST00000281456.10:c.111+13C= ENSP00000281456.5:n.111+13C=
ENST00000491736.1:c.111+13C= ENSP00000476711.1:n.111+13C=
NM_001151.3:c.111+13C= NP_001142.2:n.111+13C=
NM_001151.4:c.111+13C= MANE Select NP_001142.2:n.111+13C=