Canonical Allele Identifier: CA2395758452
Gene: SLC25A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19176881A= , CM000684.2:g.19176881A= GRCh38
NC_000022.10:g.19164394A= , CM000684.1:g.19164394A= GRCh37
NC_000022.9:g.17544394A= NCBI36
NG_033863.1:g.6983T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.596T= MANE Select ENSP00000215882.5:p.Phe199=
ENST00000215882.9:c.596T= ENSP00000215882.5:p.Phe199=
ENST00000451283.5:c.287T= ENSP00000401480.1:p.Phe96=
ENST00000461267.1:n.742T=
ENST00000470922.5:n.738T=
NM_001256534.1:c.617T= NP_001243463.1:p.Phe206=
NM_001287387.1:c.287T= NP_001274316.1:p.Phe96=
NM_005984.4:c.596T= NP_005975.1:p.Phe199=
NR_046298.2:n.647T=
NM_005984.5:c.596T= MANE Select NP_005975.1:p.Phe199=
NM_001256534.2:c.617T= NP_001243463.1:p.Phe206=
NM_001287387.2:c.287T= NP_001274316.1:p.Phe96=
NR_046298.3:n.520T=