Canonical Allele Identifier: CA2395757869
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176105C= , CM000684.2:g.19176105C= GRCh38
NC_000022.10:g.19163618C= , CM000684.1:g.19163618C= GRCh37
NC_000022.9:g.17543618C= NCBI36
NG_033863.1:g.7759G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.*25G= MANE Select ENSP00000215882.5:n.*25G=
ENST00000215882.9:c.*25G= ENSP00000215882.5:n.*25G=
ENST00000451283.5:c.*25G= ENSP00000401480.1:n.*25G=
ENST00000470922.5:n.1103G=
NM_001256534.1:c.*25G= NP_001243463.1:n.*25G=
NM_001287387.1:c.*25G= NP_001274316.1:n.*25G=
NM_005984.4:c.*25G= NP_005975.1:n.*25G=
NR_046298.2:n.1012G=
NM_005984.5:c.*25G= MANE Select NP_005975.1:n.*25G=
NM_001256534.2:c.*25G= NP_001243463.1:n.*25G=
NM_001287387.2:c.*25G= NP_001274316.1:n.*25G=
NR_046298.3:n.885G=