Canonical Allele Identifier: CA2395757957

Gene: SLC25A1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176286_19176287delinsCA , CM000684.2:g.19176286_19176287delinsCA	GRCh38
NC_000022.10:g.19163799_19163800delinsCA , CM000684.1:g.19163799_19163800delinsCA	GRCh37
NC_000022.9:g.17543799_17543800delinsCA	NCBI36
NG_033863.1:g.7577_7578delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.822-43_822-42delinsTG MANE Select	ENSP00000215882.5:n.822-43_822-42delinsTG
ENST00000215882.9:c.822-43_822-42delinsTG	ENSP00000215882.5:n.822-43_822-42delinsTG
ENST00000451283.5:c.513-43_513-42delinsTG	ENSP00000401480.1:n.513-43_513-42delinsTG
ENST00000470922.5:n.964-43_964-42delinsTG
NM_001256534.1:c.843-43_843-42delinsTG	NP_001243463.1:n.843-43_843-42delinsTG
NM_001287387.1:c.513-43_513-42delinsTG	NP_001274316.1:n.513-43_513-42delinsTG
NM_005984.4:c.822-43_822-42delinsTG	NP_005975.1:n.822-43_822-42delinsTG
NR_046298.2:n.873-43_873-42delinsTG
NM_005984.5:c.822-43_822-42delinsTG MANE Select	NP_005975.1:n.822-43_822-42delinsTG
NM_001256534.2:c.843-43_843-42delinsTG	NP_001243463.1:n.843-43_843-42delinsTG
NM_001287387.2:c.513-43_513-42delinsTG	NP_001274316.1:n.513-43_513-42delinsTG
NR_046298.3:n.746-43_746-42delinsTG