Canonical Allele Identifier: CA1519346927
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144735C= , CM000666.2:g.185144735C= GRCh38
NC_000004.11:g.186065889C= , CM000666.1:g.186065889C= GRCh37
NC_000004.10:g.186302883C= NCBI36
NG_013001.1:g.6473C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-29C= MANE Select ENSP00000281456.5:n.112-29C=
ENST00000281456.10:c.112-29C= ENSP00000281456.5:n.112-29C=
ENST00000491736.1:c.112-29C= ENSP00000476711.1:n.112-29C=
NM_001151.3:c.112-29C= NP_001142.2:n.112-29C=
NM_001151.4:c.112-29C= MANE Select NP_001142.2:n.112-29C=