Canonical Allele Identifier: CA3156427
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs778649490
ExAC: 4:186065910 TCCA / T
gnomAD v2: 4-186065910-TCCA-T
gnomAD v4: 4-185144756-TCCA-T
MyVariant Identifiers: chr4:g.186065911_186065913del (hg19) chr4:g.185144757_185144759del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144760_185144762del , CM000666.2:g.185144760_185144762del GRCh38
NC_000004.11:g.186065914_186065916del , CM000666.1:g.186065914_186065916del GRCh37
NC_000004.10:g.186302908_186302910del NCBI36
NG_013001.1:g.6498_6500del

Transcript Alleles

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