Canonical Allele Identifier: CA1519346828
Gene: SLC25A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144666A= , CM000666.2:g.185144666A= GRCh38
NC_000004.11:g.186065820A= , CM000666.1:g.186065820A= GRCh37
NC_000004.10:g.186302814A= NCBI36
NG_013001.1:g.6404A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-98A= MANE Select ENSP00000281456.5:n.112-98A=
ENST00000281456.10:c.112-98A= ENSP00000281456.5:n.112-98A=
ENST00000491736.1:c.112-98A= ENSP00000476711.1:n.112-98A=
NM_001151.3:c.112-98A= NP_001142.2:n.112-98A=
NM_001151.4:c.112-98A= MANE Select NP_001142.2:n.112-98A=