Canonical Allele Identifier: CA410637270

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164417C>G (hg19) ; chr22:g.19176904C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176904C>G , CM000684.2:g.19176904C>G	GRCh38
NC_000022.10:g.19164417C>G , CM000684.1:g.19164417C>G	GRCh37
NC_000022.9:g.17544417C>G	NCBI36
NG_033863.1:g.6960G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.573G>C MANE Select	ENSP00000215882.5:p.Gln191His
ENST00000215882.9:c.573G>C	ENSP00000215882.5:p.Gln191His
ENST00000451283.5:c.264G>C	ENSP00000401480.1:p.Gln88His
ENST00000461267.1:n.719G>C
ENST00000470922.5:n.715G>C
NM_001256534.1:c.594G>C	NP_001243463.1:p.Gln198His
NM_001287387.1:c.264G>C	NP_001274316.1:p.Gln88His
NM_005984.4:c.573G>C	NP_005975.1:p.Gln191His
NR_046298.2:n.624G>C
NM_005984.5:c.573G>C MANE Select	NP_005975.1:p.Gln191His
NM_001256534.2:c.594G>C	NP_001243463.1:p.Gln198His
NM_001287387.2:c.264G>C	NP_001274316.1:p.Gln88His
NR_046298.3:n.497G>C