Canonical Allele Identifier: CA410633867

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19163714C>A (hg19) ; chr22:g.19176201C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176201C>A , CM000684.2:g.19176201C>A	GRCh38
NC_000022.10:g.19163714C>A , CM000684.1:g.19163714C>A	GRCh37
NC_000022.9:g.17543714C>A	NCBI36
NG_033863.1:g.7663G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.865G>T MANE Select	ENSP00000215882.5:p.Asp289Tyr
ENST00000215882.9:c.865G>T	ENSP00000215882.5:p.Asp289Tyr
ENST00000451283.5:c.556G>T	ENSP00000401480.1:p.Asp186Tyr
ENST00000470922.5:n.1007G>T
NM_001256534.1:c.886G>T	NP_001243463.1:p.Asp296Tyr
NM_001287387.1:c.556G>T	NP_001274316.1:p.Asp186Tyr
NM_005984.4:c.865G>T	NP_005975.1:p.Asp289Tyr
NR_046298.2:n.916G>T
NM_005984.5:c.865G>T MANE Select	NP_005975.1:p.Asp289Tyr
NM_001256534.2:c.886G>T	NP_001243463.1:p.Asp296Tyr
NM_001287387.2:c.556G>T	NP_001274316.1:p.Asp186Tyr
NR_046298.3:n.789G>T