Canonical Allele Identifier: CA410638489

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19165251C>G (hg19) ; chr22:g.19177738C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177738C>G , CM000684.2:g.19177738C>G	GRCh38
NC_000022.10:g.19165251C>G , CM000684.1:g.19165251C>G	GRCh37
NC_000022.9:g.17545251C>G	NCBI36
NG_033805.1:g.118979G>C
NG_033863.1:g.6126G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.430G>C MANE Select	ENSP00000215882.5:p.Glu144Gln
ENST00000215882.9:c.430G>C	ENSP00000215882.5:p.Glu144Gln
ENST00000451283.5:c.121G>C	ENSP00000401480.1:p.Glu41Gln
ENST00000461267.1:n.576G>C
ENST00000470922.5:n.572G>C
NM_001256534.1:c.451G>C	NP_001243463.1:p.Glu151Gln
NM_001287387.1:c.121G>C	NP_001274316.1:p.Glu41Gln
NM_005984.4:c.430G>C	NP_005975.1:p.Glu144Gln
NR_046298.2:n.492+204G>C
NM_005984.5:c.430G>C MANE Select	NP_005975.1:p.Glu144Gln
NM_001256534.2:c.451G>C	NP_001243463.1:p.Glu151Gln
NM_001287387.2:c.121G>C	NP_001274316.1:p.Glu41Gln
NR_046298.3:n.365+204G>C