Canonical Allele Identifier: CA2395758001
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176379G= , CM000684.2:g.19176379G= GRCh38
NC_000022.10:g.19163892G= , CM000684.1:g.19163892G= GRCh37
NC_000022.9:g.17543892G= NCBI36
NG_033863.1:g.7485C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.821+42C= MANE Select ENSP00000215882.5:n.821+42C=
ENST00000215882.9:c.821+42C= ENSP00000215882.5:n.821+42C=
ENST00000451283.5:c.512+42C= ENSP00000401480.1:n.512+42C=
ENST00000470922.5:n.963+42C=
NM_001256534.1:c.842+42C= NP_001243463.1:n.842+42C=
NM_001287387.1:c.512+42C= NP_001274316.1:n.512+42C=
NM_005984.4:c.821+42C= NP_005975.1:n.821+42C=
NR_046298.2:n.872+42C=
NM_005984.5:c.821+42C= MANE Select NP_005975.1:n.821+42C=
NM_001256534.2:c.842+42C= NP_001243463.1:n.842+42C=
NM_001287387.2:c.512+42C= NP_001274316.1:n.512+42C=
NR_046298.3:n.745+42C=