Canonical Allele Identifier: CA2655261569
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177055dup , CM000684.2:g.19177055dup GRCh38
NC_000022.10:g.19164568dup , CM000684.1:g.19164568dup GRCh37
NC_000022.9:g.17544568dup NCBI36
NG_033863.1:g.6809dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.526+65dup MANE Select ENSP00000215882.5:n.526+65dup
ENST00000215882.9:c.526+65dup ENSP00000215882.5:n.526+65dup
ENST00000451283.5:c.217+65dup ENSP00000401480.1:n.217+65dup
ENST00000461267.1:n.672+65dup
ENST00000470922.5:n.668+65dup
NM_001256534.1:c.547+65dup NP_001243463.1:n.547+65dup
NM_001287387.1:c.217+65dup NP_001274316.1:n.217+65dup
NM_005984.4:c.526+65dup NP_005975.1:n.526+65dup
NR_046298.2:n.577+65dup
NM_005984.5:c.526+65dup MANE Select NP_005975.1:n.526+65dup
NM_001256534.2:c.547+65dup NP_001243463.1:n.547+65dup
NM_001287387.2:c.217+65dup NP_001274316.1:n.217+65dup
NR_046298.3:n.450+65dup