Canonical Allele Identifier: CA2395758450
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176876C= , CM000684.2:g.19176876C= GRCh38
NC_000022.10:g.19164389C= , CM000684.1:g.19164389C= GRCh37
NC_000022.9:g.17544389C= NCBI36
NG_033863.1:g.6988G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.601G= MANE Select ENSP00000215882.5:p.Val201=
ENST00000215882.9:c.601G= ENSP00000215882.5:p.Val201=
ENST00000451283.5:c.292G= ENSP00000401480.1:p.Val98=
ENST00000461267.1:n.747G=
ENST00000470922.5:n.743G=
NM_001256534.1:c.622G= NP_001243463.1:p.Val208=
NM_001287387.1:c.292G= NP_001274316.1:p.Val98=
NM_005984.4:c.601G= NP_005975.1:p.Val201=
NR_046298.2:n.652G=
NM_005984.5:c.601G= MANE Select NP_005975.1:p.Val201=
NM_001256534.2:c.622G= NP_001243463.1:p.Val208=
NM_001287387.2:c.292G= NP_001274316.1:p.Val98=
NR_046298.3:n.525G=