Canonical Allele Identifier: CA513188100
Gene: SLC25A1 HGNC NCBI

Linked Data

dbSNP Id: rs1398003720

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176892C>T , CM000684.2:g.19176892C>T GRCh38
NC_000022.10:g.19164405C>T , CM000684.1:g.19164405C>T GRCh37
NC_000022.9:g.17544405C>T NCBI36
NG_033863.1:g.6972G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.585G>A MANE Select ENSP00000215882.5:p.Gln195=
ENST00000215882.9:c.585G>A ENSP00000215882.5:p.Gln195=
ENST00000451283.5:c.276G>A ENSP00000401480.1:p.Gln92=
ENST00000461267.1:n.731G>A
ENST00000470922.5:n.727G>A
NM_001256534.1:c.606G>A NP_001243463.1:p.Gln202=
NM_001287387.1:c.276G>A NP_001274316.1:p.Gln92=
NM_005984.4:c.585G>A NP_005975.1:p.Gln195=
NR_046298.2:n.636G>A
NM_005984.5:c.585G>A MANE Select NP_005975.1:p.Gln195=
NM_001256534.2:c.606G>A NP_001243463.1:p.Gln202=
NM_001287387.2:c.276G>A NP_001274316.1:p.Gln92=
NR_046298.3:n.509G>A