Canonical Allele Identifier: CA2395758779
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177693G= , CM000684.2:g.19177693G= GRCh38
NC_000022.10:g.19165206G= , CM000684.1:g.19165206G= GRCh37
NC_000022.9:g.17545206G= NCBI36
NG_033805.1:g.119024C=
NG_033863.1:g.6171C=

Transcript Alleles

HGVS Amino-acid change
ENST00000215882.10:c.441+34C= MANE Select ENSP00000215882.5:n.441+34C=
ENST00000215882.9:c.441+34C= ENSP00000215882.5:n.441+34C=
ENST00000451283.5:c.132+34C= ENSP00000401480.1:n.132+34C=
ENST00000461267.1:n.587+34C=
ENST00000470922.5:n.583+34C=
NM_001256534.1:c.462+34C= NP_001243463.1:n.462+34C=
NM_001287387.1:c.132+34C= NP_001274316.1:n.132+34C=
NM_005984.4:c.441+34C= NP_005975.1:n.441+34C=
NR_046298.2:n.492+249C=
NM_005984.5:c.441+34C= MANE Select NP_005975.1:n.441+34C=
NM_001256534.2:c.462+34C= NP_001243463.1:n.462+34C=
NM_001287387.2:c.132+34C= NP_001274316.1:n.132+34C=
NR_046298.3:n.365+249C=