Canonical Allele Identifier: CA2395757882
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176121T= , CM000684.2:g.19176121T= GRCh38
NC_000022.10:g.19163634T= , CM000684.1:g.19163634T= GRCh37
NC_000022.9:g.17543634T= NCBI36
NG_033863.1:g.7743A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.*9A= MANE Select ENSP00000215882.5:n.*9A=
ENST00000215882.9:c.*9A= ENSP00000215882.5:n.*9A=
ENST00000451283.5:c.*9A= ENSP00000401480.1:n.*9A=
ENST00000470922.5:n.1087A=
NM_001256534.1:c.*9A= NP_001243463.1:n.*9A=
NM_001287387.1:c.*9A= NP_001274316.1:n.*9A=
NM_005984.4:c.*9A= NP_005975.1:n.*9A=
NR_046298.2:n.996A=
NM_005984.5:c.*9A= MANE Select NP_005975.1:n.*9A=
NM_001256534.2:c.*9A= NP_001243463.1:n.*9A=
NM_001287387.2:c.*9A= NP_001274316.1:n.*9A=
NR_046298.3:n.869A=