Canonical Allele Identifier: CA557394844
Gene: SLC25A4 HGNC NCBI

Linked Data

gnomAD v2: 4-186065860-TCC-T
gnomAD v3: 4-185144706-TCC-T
gnomAD v4: 4-185144706-TCC-T
MyVariant Identifiers: chr4:g.186065861_186065862del (hg19) chr4:g.185144707_185144708del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144707_185144708del , CM000666.2:g.185144707_185144708del GRCh38
NC_000004.11:g.186065861_186065862del , CM000666.1:g.186065861_186065862del GRCh37
NC_000004.10:g.186302855_186302856del NCBI36
NG_013001.1:g.6445_6446del

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-57_112-56del MANE Select ENSP00000281456.5:n.112-57_112-56del
ENST00000281456.10:c.112-57_112-56del ENSP00000281456.5:n.112-57_112-56del
ENST00000491736.1:c.112-57_112-56del ENSP00000476711.1:n.112-57_112-56del
NM_001151.3:c.112-57_112-56del NP_001142.2:n.112-57_112-56del
NM_001151.4:c.112-57_112-56del MANE Select NP_001142.2:n.112-57_112-56del
Search 100 bp 5'
Search 100 bp 3'