Canonical Allele Identifier: CA2395757877
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176113T= , CM000684.2:g.19176113T= GRCh38
NC_000022.10:g.19163626T= , CM000684.1:g.19163626T= GRCh37
NC_000022.9:g.17543626T= NCBI36
NG_033863.1:g.7751A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.*17A= MANE Select ENSP00000215882.5:n.*17A=
ENST00000215882.9:c.*17A= ENSP00000215882.5:n.*17A=
ENST00000451283.5:c.*17A= ENSP00000401480.1:n.*17A=
ENST00000470922.5:n.1095A=
NM_001256534.1:c.*17A= NP_001243463.1:n.*17A=
NM_001287387.1:c.*17A= NP_001274316.1:n.*17A=
NM_005984.4:c.*17A= NP_005975.1:n.*17A=
NR_046298.2:n.1004A=
NM_005984.5:c.*17A= MANE Select NP_005975.1:n.*17A=
NM_001256534.2:c.*17A= NP_001243463.1:n.*17A=
NM_001287387.2:c.*17A= NP_001274316.1:n.*17A=
NR_046298.3:n.877A=