Canonical Allele Identifier: CA2395758789
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177702G= , CM000684.2:g.19177702G= GRCh38
NC_000022.10:g.19165215G= , CM000684.1:g.19165215G= GRCh37
NC_000022.9:g.17545215G= NCBI36
NG_033805.1:g.119015C=
NG_033863.1:g.6162C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.441+25C= MANE Select ENSP00000215882.5:n.441+25C=
ENST00000215882.9:c.441+25C= ENSP00000215882.5:n.441+25C=
ENST00000451283.5:c.132+25C= ENSP00000401480.1:n.132+25C=
ENST00000461267.1:n.587+25C=
ENST00000470922.5:n.583+25C=
NM_001256534.1:c.462+25C= NP_001243463.1:n.462+25C=
NM_001287387.1:c.132+25C= NP_001274316.1:n.132+25C=
NM_005984.4:c.441+25C= NP_005975.1:n.441+25C=
NR_046298.2:n.492+240C=
NM_005984.5:c.441+25C= MANE Select NP_005975.1:n.441+25C=
NM_001256534.2:c.462+25C= NP_001243463.1:n.462+25C=
NM_001287387.2:c.132+25C= NP_001274316.1:n.132+25C=
NR_046298.3:n.365+240C=