Canonical Allele Identifier: CA2395758478
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176940C= , CM000684.2:g.19176940C= GRCh38
NC_000022.10:g.19164453C= , CM000684.1:g.19164453C= GRCh37
NC_000022.9:g.17544453C= NCBI36
NG_033863.1:g.6924G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.537G= MANE Select ENSP00000215882.5:p.Gly179=
ENST00000215882.9:c.537G= ENSP00000215882.5:p.Gly179=
ENST00000451283.5:c.228G= ENSP00000401480.1:p.Gly76=
ENST00000461267.1:n.683G=
ENST00000470922.5:n.679G=
NM_001256534.1:c.558G= NP_001243463.1:p.Gly186=
NM_001287387.1:c.228G= NP_001274316.1:p.Gly76=
NM_005984.4:c.537G= NP_005975.1:p.Gly179=
NR_046298.2:n.588G=
NM_005984.5:c.537G= MANE Select NP_005975.1:p.Gly179=
NM_001256534.2:c.558G= NP_001243463.1:p.Gly186=
NM_001287387.2:c.228G= NP_001274316.1:p.Gly76=
NR_046298.3:n.461G=