Canonical Allele Identifier: CA917385917
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs34795113

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144698_185144699dup , CM000666.2:g.185144698_185144699dup GRCh38
NC_000004.11:g.186065852_186065853dup , CM000666.1:g.186065852_186065853dup GRCh37
NC_000004.10:g.186302846_186302847dup NCBI36
NG_013001.1:g.6436_6437dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-66_112-65dup MANE Select ENSP00000281456.5:n.112-66_112-65dup
ENST00000281456.10:c.112-66_112-65dup ENSP00000281456.5:n.112-66_112-65dup
ENST00000491736.1:c.112-66_112-65dup ENSP00000476711.1:n.112-66_112-65dup
NM_001151.3:c.112-66_112-65dup NP_001142.2:n.112-66_112-65dup
NM_001151.4:c.112-66_112-65dup MANE Select NP_001142.2:n.112-66_112-65dup