Canonical Allele Identifier: CA2655261395
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176348_19176370dup , CM000684.2:g.19176348_19176370dup GRCh38
NC_000022.10:g.19163861_19163883dup , CM000684.1:g.19163861_19163883dup GRCh37
NC_000022.9:g.17543861_17543883dup NCBI36
NG_033863.1:g.7496_7518dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.821+53_821+75dup MANE Select ENSP00000215882.5:n.821+53_821+75dup
ENST00000215882.9:c.821+53_821+75dup ENSP00000215882.5:n.821+53_821+75dup
ENST00000451283.5:c.512+53_512+75dup ENSP00000401480.1:n.512+53_512+75dup
ENST00000470922.5:n.963+53_963+75dup
NM_001256534.1:c.842+53_842+75dup NP_001243463.1:n.842+53_842+75dup
NM_001287387.1:c.512+53_512+75dup NP_001274316.1:n.512+53_512+75dup
NM_005984.4:c.821+53_821+75dup NP_005975.1:n.821+53_821+75dup
NR_046298.2:n.872+53_872+75dup
NM_005984.5:c.821+53_821+75dup MANE Select NP_005975.1:n.821+53_821+75dup
NM_001256534.2:c.842+53_842+75dup NP_001243463.1:n.842+53_842+75dup
NM_001287387.2:c.512+53_512+75dup NP_001274316.1:n.512+53_512+75dup
NR_046298.3:n.745+53_745+75dup