Canonical Allele Identifier: CA638503425

Gene: SLC25A1

Linked Data

• dbSNP Id: rs1320807995
• gnomAD v2: 22-19163623-C-T
• gnomAD v3: 22-19176110-C-T
• gnomAD v4: 22-19176110-C-T
• MyVariant Identifiers: chr22:g.19163623C>T (hg19) ; chr22:g.19176110C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176110C>T , CM000684.2:g.19176110C>T	GRCh38
NC_000022.10:g.19163623C>T , CM000684.1:g.19163623C>T	GRCh37
NC_000022.9:g.17543623C>T	NCBI36
NG_033863.1:g.7754G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.*20G>A MANE Select	ENSP00000215882.5:n.*20G>A
ENST00000215882.9:c.*20G>A	ENSP00000215882.5:n.*20G>A
ENST00000451283.5:c.*20G>A	ENSP00000401480.1:n.*20G>A
ENST00000470922.5:n.1098G>A
NM_001256534.1:c.*20G>A	NP_001243463.1:n.*20G>A
NM_001287387.1:c.*20G>A	NP_001274316.1:n.*20G>A
NM_005984.4:c.*20G>A	NP_005975.1:n.*20G>A
NR_046298.2:n.1007G>A
NM_005984.5:c.*20G>A MANE Select	NP_005975.1:n.*20G>A
NM_001256534.2:c.*20G>A	NP_001243463.1:n.*20G>A
NM_001287387.2:c.*20G>A	NP_001274316.1:n.*20G>A
NR_046298.3:n.880G>A