Canonical Allele Identifier: CA1071902642
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1734405669

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144690_185144691insG , CM000666.2:g.185144690_185144691insG GRCh38
NC_000004.11:g.186065844_186065845insG , CM000666.1:g.186065844_186065845insG GRCh37
NC_000004.10:g.186302838_186302839insG NCBI36
NG_013001.1:g.6428_6429insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-74_112-73insG MANE Select ENSP00000281456.5:n.112-74_112-73insG
ENST00000281456.10:c.112-74_112-73insG ENSP00000281456.5:n.112-74_112-73insG
ENST00000491736.1:c.112-74_112-73insG ENSP00000476711.1:n.112-74_112-73insG
NM_001151.3:c.112-74_112-73insG NP_001142.2:n.112-74_112-73insG
NM_001151.4:c.112-74_112-73insG MANE Select NP_001142.2:n.112-74_112-73insG