Canonical Allele Identifier: CA410636658

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164183T>A (hg19) ; chr22:g.19176670T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176670T>A , CM000684.2:g.19176670T>A	GRCh38
NC_000022.10:g.19164183T>A , CM000684.1:g.19164183T>A	GRCh37
NC_000022.9:g.17544183T>A	NCBI36
NG_033863.1:g.7194A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.655A>T MANE Select	ENSP00000215882.5:p.Asn219Tyr
ENST00000215882.9:c.655A>T	ENSP00000215882.5:p.Asn219Tyr
ENST00000451283.5:c.346A>T	ENSP00000401480.1:p.Asn116Tyr
ENST00000461267.1:n.801A>T
ENST00000470922.5:n.797A>T
NM_001256534.1:c.676A>T	NP_001243463.1:p.Asn226Tyr
NM_001287387.1:c.346A>T	NP_001274316.1:p.Asn116Tyr
NM_005984.4:c.655A>T	NP_005975.1:p.Asn219Tyr
NR_046298.2:n.706A>T
NM_005984.5:c.655A>T MANE Select	NP_005975.1:p.Asn219Tyr
NM_001256534.2:c.676A>T	NP_001243463.1:p.Asn226Tyr
NM_001287387.2:c.346A>T	NP_001274316.1:p.Asn116Tyr
NR_046298.3:n.579A>T