Canonical Allele Identifier: CA1519347106
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144886G= , CM000666.2:g.185144886G= GRCh38
NC_000004.11:g.186066040G= , CM000666.1:g.186066040G= GRCh37
NC_000004.10:g.186303034G= NCBI36
NG_013001.1:g.6624G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.234G= MANE Select ENSP00000281456.5:p.Val78=
ENST00000281456.10:c.234G= ENSP00000281456.5:p.Val78=
ENST00000491736.1:c.234G= ENSP00000476711.1:p.Val78=
NM_001151.3:c.234G= NP_001142.2:p.Val78=
NM_001151.4:c.234G= MANE Select NP_001142.2:p.Val78=