Canonical Allele Identifier: CA10097412

Gene: SLC25A1

Linked Data

• dbSNP Id: rs782664379
• ExAC: 22:19164512 T / C
• gnomAD v2: 22-19164512-T-C
• gnomAD v4: 22-19176999-T-C
• MyVariant Identifiers: chr22:g.19164512T>C (hg19) ; chr22:g.19176999T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176999T>C , CM000684.2:g.19176999T>C	GRCh38
NC_000022.10:g.19164512T>C , CM000684.1:g.19164512T>C	GRCh37
NC_000022.9:g.17544512T>C	NCBI36
NG_033863.1:g.6865A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.527-49A>G MANE Select	ENSP00000215882.5:n.527-49A>G
ENST00000215882.9:c.527-49A>G	ENSP00000215882.5:n.527-49A>G
ENST00000451283.5:c.218-49A>G	ENSP00000401480.1:n.218-49A>G
ENST00000461267.1:n.673-49A>G
ENST00000470922.5:n.669-49A>G
NM_001256534.1:c.548-49A>G	NP_001243463.1:n.548-49A>G
NM_001287387.1:c.218-49A>G	NP_001274316.1:n.218-49A>G
NM_005984.4:c.527-49A>G	NP_005975.1:n.527-49A>G
NR_046298.2:n.578-49A>G
NM_005984.5:c.527-49A>G MANE Select	NP_005975.1:n.527-49A>G
NM_001256534.2:c.548-49A>G	NP_001243463.1:n.548-49A>G
NM_001287387.2:c.218-49A>G	NP_001274316.1:n.218-49A>G
NR_046298.3:n.451-49A>G