Canonical Allele Identifier: CA2395758711

Gene: SLC25A1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177595_19177596delinsAC , CM000684.2:g.19177595_19177596delinsAC	GRCh38
NC_000022.10:g.19165108_19165109delinsAC , CM000684.1:g.19165108_19165109delinsAC	GRCh37
NC_000022.9:g.17545108_17545109delinsAC	NCBI36
NG_033805.1:g.119121_119122delinsGT
NG_033863.1:g.6268_6269delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.441+131_441+132delinsGT MANE Select	ENSP00000215882.5:n.441+131_441+132delinsGT
ENST00000215882.9:c.441+131_441+132delinsGT	ENSP00000215882.5:n.441+131_441+132delinsGT
ENST00000451283.5:c.132+131_132+132delinsGT	ENSP00000401480.1:n.132+131_132+132delinsGT
ENST00000461267.1:n.587+131_587+132delinsGT
ENST00000470922.5:n.583+131_583+132delinsGT
NM_001256534.1:c.462+131_462+132delinsGT	NP_001243463.1:n.462+131_462+132delinsGT
NM_001287387.1:c.132+131_132+132delinsGT	NP_001274316.1:n.132+131_132+132delinsGT
NM_005984.4:c.441+131_441+132delinsGT	NP_005975.1:n.441+131_441+132delinsGT
NR_046298.2:n.492+346_492+347delinsGT
NM_005984.5:c.441+131_441+132delinsGT MANE Select	NP_005975.1:n.441+131_441+132delinsGT
NM_001256534.2:c.462+131_462+132delinsGT	NP_001243463.1:n.462+131_462+132delinsGT
NM_001287387.2:c.132+131_132+132delinsGT	NP_001274316.1:n.132+131_132+132delinsGT
NR_046298.3:n.365+346_365+347delinsGT