Canonical Allele Identifier: CA2395757901
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176163C= , CM000684.2:g.19176163C= GRCh38
NC_000022.10:g.19163676C= , CM000684.1:g.19163676C= GRCh37
NC_000022.9:g.17543676C= NCBI36
NG_033863.1:g.7701G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.903G= MANE Select ENSP00000215882.5:p.Val301=
ENST00000215882.9:c.903G= ENSP00000215882.5:p.Val301=
ENST00000451283.5:c.594G= ENSP00000401480.1:p.Val198=
ENST00000470922.5:n.1045G=
NM_001256534.1:c.924G= NP_001243463.1:p.Val308=
NM_001287387.1:c.594G= NP_001274316.1:p.Val198=
NM_005984.4:c.903G= NP_005975.1:p.Val301=
NR_046298.2:n.954G=
NM_005984.5:c.903G= MANE Select NP_005975.1:p.Val301=
NM_001256534.2:c.924G= NP_001243463.1:p.Val308=
NM_001287387.2:c.594G= NP_001274316.1:p.Val198=
NR_046298.3:n.827G=