Canonical Allele Identifier: CA917385914
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1560841540

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144646_185144648del , CM000666.2:g.185144646_185144648del GRCh38
NC_000004.11:g.186065800_186065802del , CM000666.1:g.186065800_186065802del GRCh37
NC_000004.10:g.186302794_186302796del NCBI36
NG_013001.1:g.6384_6386del

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-118_112-116del MANE Select ENSP00000281456.5:n.112-118_112-116del
ENST00000281456.10:c.112-118_112-116del ENSP00000281456.5:n.112-118_112-116del
ENST00000491736.1:c.112-118_112-116del ENSP00000476711.1:n.112-118_112-116del
NM_001151.3:c.112-118_112-116del NP_001142.2:n.112-118_112-116del
NM_001151.4:c.112-118_112-116del MANE Select NP_001142.2:n.112-118_112-116del