Canonical Allele Identifier: CA1519346877
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1734406082

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144703_185144704del , CM000666.2:g.185144703_185144704del GRCh38
NC_000004.11:g.186065857_186065858del , CM000666.1:g.186065857_186065858del GRCh37
NC_000004.10:g.186302851_186302852del NCBI36
NG_013001.1:g.6441_6442del

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-61_112-60del MANE Select ENSP00000281456.5:n.112-61_112-60del
ENST00000281456.10:c.112-61_112-60del ENSP00000281456.5:n.112-61_112-60del
ENST00000491736.1:c.112-61_112-60del ENSP00000476711.1:n.112-61_112-60del
NM_001151.3:c.112-61_112-60del NP_001142.2:n.112-61_112-60del
NM_001151.4:c.112-61_112-60del MANE Select NP_001142.2:n.112-61_112-60del