Canonical Allele Identifier: CA2395758172

Gene: SLC25A1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176557T= , CM000684.2:g.19176557T=	GRCh38
NC_000022.10:g.19164070T= , CM000684.1:g.19164070T=	GRCh37
NC_000022.9:g.17544070T=	NCBI36
NG_033863.1:g.7307A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.747+21A= MANE Select	ENSP00000215882.5:n.747+21A=
ENST00000215882.9:c.747+21A=	ENSP00000215882.5:n.747+21A=
ENST00000451283.5:c.438+21A=	ENSP00000401480.1:n.438+21A=
ENST00000470922.5:n.889+21A=
NM_001256534.1:c.768+21A=	NP_001243463.1:n.768+21A=
NM_001287387.1:c.438+21A=	NP_001274316.1:n.438+21A=
NM_005984.4:c.747+21A=	NP_005975.1:n.747+21A=
NR_046298.2:n.798+21A=
NM_005984.5:c.747+21A= MANE Select	NP_005975.1:n.747+21A=
NM_001256534.2:c.768+21A=	NP_001243463.1:n.768+21A=
NM_001287387.2:c.438+21A=	NP_001274316.1:n.438+21A=
NR_046298.3:n.671+21A=