Canonical Allele Identifier: CA2395758006

Gene: SLC25A1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176394_19176395delinsCA , CM000684.2:g.19176394_19176395delinsCA	GRCh38
NC_000022.10:g.19163907_19163908delinsCA , CM000684.1:g.19163907_19163908delinsCA	GRCh37
NC_000022.9:g.17543907_17543908delinsCA	NCBI36
NG_033863.1:g.7469_7470delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.821+26_821+27delinsTG MANE Select	ENSP00000215882.5:n.821+26_821+27delinsTG
ENST00000215882.9:c.821+26_821+27delinsTG	ENSP00000215882.5:n.821+26_821+27delinsTG
ENST00000451283.5:c.512+26_512+27delinsTG	ENSP00000401480.1:n.512+26_512+27delinsTG
ENST00000470922.5:n.963+26_963+27delinsTG
NM_001256534.1:c.842+26_842+27delinsTG	NP_001243463.1:n.842+26_842+27delinsTG
NM_001287387.1:c.512+26_512+27delinsTG	NP_001274316.1:n.512+26_512+27delinsTG
NM_005984.4:c.821+26_821+27delinsTG	NP_005975.1:n.821+26_821+27delinsTG
NR_046298.2:n.872+26_872+27delinsTG
NM_005984.5:c.821+26_821+27delinsTG MANE Select	NP_005975.1:n.821+26_821+27delinsTG
NM_001256534.2:c.842+26_842+27delinsTG	NP_001243463.1:n.842+26_842+27delinsTG
NM_001287387.2:c.512+26_512+27delinsTG	NP_001274316.1:n.512+26_512+27delinsTG
NR_046298.3:n.745+26_745+27delinsTG