Canonical Allele Identifier: CA410635812

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164090C>T (hg19) ; chr22:g.19176577C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176577C>T , CM000684.2:g.19176577C>T	GRCh38
NC_000022.10:g.19164090C>T , CM000684.1:g.19164090C>T	GRCh37
NC_000022.9:g.17544090C>T	NCBI36
NG_033863.1:g.7287G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000215882.10:c.747+1G>A MANE Select	ENSP00000215882.5:n.747+1G>A
ENST00000215882.9:c.747+1G>A	ENSP00000215882.5:n.747+1G>A
ENST00000451283.5:c.438+1G>A	ENSP00000401480.1:n.438+1G>A
ENST00000470922.5:n.889+1G>A
NM_001256534.1:c.768+1G>A	NP_001243463.1:n.768+1G>A
NM_001287387.1:c.438+1G>A	NP_001274316.1:n.438+1G>A
NM_005984.4:c.747+1G>A	NP_005975.1:n.747+1G>A
NR_046298.2:n.798+1G>A
NM_005984.5:c.747+1G>A MANE Select	NP_005975.1:n.747+1G>A
NM_001256534.2:c.768+1G>A	NP_001243463.1:n.768+1G>A
NM_001287387.2:c.438+1G>A	NP_001274316.1:n.438+1G>A
NR_046298.3:n.671+1G>A