Canonical Allele Identifier: CA917385916
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1560841550
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144663_185144664insCA , CM000666.2:g.185144663_185144664insCA GRCh38
NC_000004.11:g.186065817_186065818insCA , CM000666.1:g.186065817_186065818insCA GRCh37
NC_000004.10:g.186302811_186302812insCA NCBI36
NG_013001.1:g.6401_6402insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-101_112-100insCA MANE Select ENSP00000281456.5:n.112-101_112-100insCA
ENST00000281456.10:c.112-101_112-100insCA ENSP00000281456.5:n.112-101_112-100insCA
ENST00000491736.1:c.112-101_112-100insCA ENSP00000476711.1:n.112-101_112-100insCA
NM_001151.3:c.112-101_112-100insCA NP_001142.2:n.112-101_112-100insCA
NM_001151.4:c.112-101_112-100insCA MANE Select NP_001142.2:n.112-101_112-100insCA
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