Canonical Allele Identifier: CA2395758784

Gene: SLC25A1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177698T= , CM000684.2:g.19177698T=	GRCh38
NC_000022.10:g.19165211T= , CM000684.1:g.19165211T=	GRCh37
NC_000022.9:g.17545211T=	NCBI36
NG_033805.1:g.119019A=
NG_033863.1:g.6166A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.441+29A= MANE Select	ENSP00000215882.5:n.441+29A=
ENST00000215882.9:c.441+29A=	ENSP00000215882.5:n.441+29A=
ENST00000451283.5:c.132+29A=	ENSP00000401480.1:n.132+29A=
ENST00000461267.1:n.587+29A=
ENST00000470922.5:n.583+29A=
NM_001256534.1:c.462+29A=	NP_001243463.1:n.462+29A=
NM_001287387.1:c.132+29A=	NP_001274316.1:n.132+29A=
NM_005984.4:c.441+29A=	NP_005975.1:n.441+29A=
NR_046298.2:n.492+244A=
NM_005984.5:c.441+29A= MANE Select	NP_005975.1:n.441+29A=
NM_001256534.2:c.462+29A=	NP_001243463.1:n.462+29A=
NM_001287387.2:c.132+29A=	NP_001274316.1:n.132+29A=
NR_046298.3:n.365+244A=