Canonical Allele Identifier: CA2655261558
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177033_19177057del , CM000684.2:g.19177033_19177057del GRCh38
NC_000022.10:g.19164546_19164570del , CM000684.1:g.19164546_19164570del GRCh37
NC_000022.9:g.17544546_17544570del NCBI36
NG_033863.1:g.6807_6831del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.526+63_527-83del MANE Select ENSP00000215882.5:n.526+63_527-83del
ENST00000215882.9:c.526+63_527-83del ENSP00000215882.5:n.526+63_527-83del
ENST00000451283.5:c.217+63_218-83del ENSP00000401480.1:n.217+63_218-83del
ENST00000461267.1:n.672+63_673-83del
ENST00000470922.5:n.668+63_669-83del
NM_001256534.1:c.547+63_548-83del NP_001243463.1:n.547+63_548-83del
NM_001287387.1:c.217+63_218-83del NP_001274316.1:n.217+63_218-83del
NM_005984.4:c.526+63_527-83del NP_005975.1:n.526+63_527-83del
NR_046298.2:n.577+63_578-83del
NM_005984.5:c.526+63_527-83del MANE Select NP_005975.1:n.526+63_527-83del
NM_001256534.2:c.547+63_548-83del NP_001243463.1:n.547+63_548-83del
NM_001287387.2:c.217+63_218-83del NP_001274316.1:n.217+63_218-83del
NR_046298.3:n.450+63_451-83del