Canonical Allele Identifier: CA1519345351
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143288T= , CM000666.2:g.185143288T= GRCh38
NC_000004.11:g.186064442T= , CM000666.1:g.186064442T= GRCh37
NC_000004.10:g.186301436T= NCBI36
NG_013001.1:g.5026T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.-85T= MANE Select ENSP00000281456.5:n.-85T=
ENST00000281456.10:c.-85T= ENSP00000281456.5:n.-85T=
ENST00000491736.1:c.-85T= ENSP00000476711.1:n.-85T=
NM_001151.3:c.-85T= NP_001142.2:n.-85T=
NM_001151.4:c.-85T= MANE Select NP_001142.2:n.-85T=