Canonical Allele Identifier: CA2395758314
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176639A= , CM000684.2:g.19176639A= GRCh38
NC_000022.10:g.19164152A= , CM000684.1:g.19164152A= GRCh37
NC_000022.9:g.17544152A= NCBI36
NG_033863.1:g.7225T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.686T= MANE Select ENSP00000215882.5:p.Ile229=
ENST00000215882.9:c.686T= ENSP00000215882.5:p.Ile229=
ENST00000451283.5:c.377T= ENSP00000401480.1:p.Ile126=
ENST00000470922.5:n.828T=
NM_001256534.1:c.707T= NP_001243463.1:p.Ile236=
NM_001287387.1:c.377T= NP_001274316.1:p.Ile126=
NM_005984.4:c.686T= NP_005975.1:p.Ile229=
NR_046298.2:n.737T=
NM_005984.5:c.686T= MANE Select NP_005975.1:p.Ile229=
NM_001256534.2:c.707T= NP_001243463.1:p.Ile236=
NM_001287387.2:c.377T= NP_001274316.1:p.Ile126=
NR_046298.3:n.610T=