Canonical Allele Identifier: CA410634629

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19163976C>G (hg19) ; chr22:g.19176463C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176463C>G , CM000684.2:g.19176463C>G	GRCh38
NC_000022.10:g.19163976C>G , CM000684.1:g.19163976C>G	GRCh37
NC_000022.9:g.17543976C>G	NCBI36
NG_033863.1:g.7401G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.779G>C MANE Select	ENSP00000215882.5:p.Trp260Ser
ENST00000215882.9:c.779G>C	ENSP00000215882.5:p.Trp260Ser
ENST00000451283.5:c.470G>C	ENSP00000401480.1:p.Trp157Ser
ENST00000470922.5:n.921G>C
NM_001256534.1:c.800G>C	NP_001243463.1:p.Trp267Ser
NM_001287387.1:c.470G>C	NP_001274316.1:p.Trp157Ser
NM_005984.4:c.779G>C	NP_005975.1:p.Trp260Ser
NR_046298.2:n.830G>C
NM_005984.5:c.779G>C MANE Select	NP_005975.1:p.Trp260Ser
NM_001256534.2:c.800G>C	NP_001243463.1:p.Trp267Ser
NM_001287387.2:c.470G>C	NP_001274316.1:p.Trp157Ser
NR_046298.3:n.703G>C