Canonical Allele Identifier: CA2395758052
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176471C= , CM000684.2:g.19176471C= GRCh38
NC_000022.10:g.19163984C= , CM000684.1:g.19163984C= GRCh37
NC_000022.9:g.17543984C= NCBI36
NG_033863.1:g.7393G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.771G= MANE Select ENSP00000215882.5:p.Arg257=
ENST00000215882.9:c.771G= ENSP00000215882.5:p.Arg257=
ENST00000451283.5:c.462G= ENSP00000401480.1:p.Arg154=
ENST00000470922.5:n.913G=
NM_001256534.1:c.792G= NP_001243463.1:p.Arg264=
NM_001287387.1:c.462G= NP_001274316.1:p.Arg154=
NM_005984.4:c.771G= NP_005975.1:p.Arg257=
NR_046298.2:n.822G=
NM_005984.5:c.771G= MANE Select NP_005975.1:p.Arg257=
NM_001256534.2:c.792G= NP_001243463.1:p.Arg264=
NM_001287387.2:c.462G= NP_001274316.1:p.Arg154=
NR_046298.3:n.695G=