Canonical Allele Identifier: CA513188100

Gene: SLC25A1

Linked Data

• dbSNP Id: rs1398003720
• gnomAD v2: 22-19164405-C-T
• gnomAD v4: 22-19176892-C-T
• MyVariant Identifiers: chr22:g.19164405C>T (hg19) ; chr22:g.19176892C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176892C>T , CM000684.2:g.19176892C>T	GRCh38
NC_000022.10:g.19164405C>T , CM000684.1:g.19164405C>T	GRCh37
NC_000022.9:g.17544405C>T	NCBI36
NG_033863.1:g.6972G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.585G>A MANE Select	ENSP00000215882.5:p.Gln195=
ENST00000215882.9:c.585G>A	ENSP00000215882.5:p.Gln195=
ENST00000451283.5:c.276G>A	ENSP00000401480.1:p.Gln92=
ENST00000461267.1:n.731G>A
ENST00000470922.5:n.727G>A
NM_001256534.1:c.606G>A	NP_001243463.1:p.Gln202=
NM_001287387.1:c.276G>A	NP_001274316.1:p.Gln92=
NM_005984.4:c.585G>A	NP_005975.1:p.Gln195=
NR_046298.2:n.636G>A
NM_005984.5:c.585G>A MANE Select	NP_005975.1:p.Gln195=
NM_001256534.2:c.606G>A	NP_001243463.1:p.Gln202=
NM_001287387.2:c.276G>A	NP_001274316.1:p.Gln92=
NR_046298.3:n.509G>A