Canonical Allele Identifier: CA2818380989

Gene: SLC25A1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176988_19176989del , CM000684.2:g.19176988_19176989del	GRCh38
NC_000022.10:g.19164501_19164502del , CM000684.1:g.19164501_19164502del	GRCh37
NC_000022.9:g.17544501_17544502del	NCBI36
NG_033863.1:g.6878_6879del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.527-36_527-35del MANE Select	ENSP00000215882.5:n.527-36_527-35del
ENST00000215882.9:c.527-36_527-35del	ENSP00000215882.5:n.527-36_527-35del
ENST00000451283.5:c.218-36_218-35del	ENSP00000401480.1:n.218-36_218-35del
ENST00000461267.1:n.673-36_673-35del
ENST00000470922.5:n.669-36_669-35del
NM_001256534.1:c.548-36_548-35del	NP_001243463.1:n.548-36_548-35del
NM_001287387.1:c.218-36_218-35del	NP_001274316.1:n.218-36_218-35del
NM_005984.4:c.527-36_527-35del	NP_005975.1:n.527-36_527-35del
NR_046298.2:n.578-36_578-35del
NM_005984.5:c.527-36_527-35del MANE Select	NP_005975.1:n.527-36_527-35del
NM_001256534.2:c.548-36_548-35del	NP_001243463.1:n.548-36_548-35del
NM_001287387.2:c.218-36_218-35del	NP_001274316.1:n.218-36_218-35del
NR_046298.3:n.451-36_451-35del