Canonical Allele Identifier: CA1519346889
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144707C= , CM000666.2:g.185144707C= GRCh38
NC_000004.11:g.186065861C= , CM000666.1:g.186065861C= GRCh37
NC_000004.10:g.186302855C= NCBI36
NG_013001.1:g.6445C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-57C= MANE Select ENSP00000281456.5:n.112-57C=
ENST00000281456.10:c.112-57C= ENSP00000281456.5:n.112-57C=
ENST00000491736.1:c.112-57C= ENSP00000476711.1:n.112-57C=
NM_001151.3:c.112-57C= NP_001142.2:n.112-57C=
NM_001151.4:c.112-57C= MANE Select NP_001142.2:n.112-57C=