Canonical Allele Identifier: CA410637199

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164400A>G (hg19) ; chr22:g.19176887A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176887A>G , CM000684.2:g.19176887A>G	GRCh38
NC_000022.10:g.19164400A>G , CM000684.1:g.19164400A>G	GRCh37
NC_000022.9:g.17544400A>G	NCBI36
NG_033863.1:g.6977T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.590T>C MANE Select	ENSP00000215882.5:p.Ile197Thr
ENST00000215882.9:c.590T>C	ENSP00000215882.5:p.Ile197Thr
ENST00000451283.5:c.281T>C	ENSP00000401480.1:p.Ile94Thr
ENST00000461267.1:n.736T>C
ENST00000470922.5:n.732T>C
NM_001256534.1:c.611T>C	NP_001243463.1:p.Ile204Thr
NM_001287387.1:c.281T>C	NP_001274316.1:p.Ile94Thr
NM_005984.4:c.590T>C	NP_005975.1:p.Ile197Thr
NR_046298.2:n.641T>C
NM_005984.5:c.590T>C MANE Select	NP_005975.1:p.Ile197Thr
NM_001256534.2:c.611T>C	NP_001243463.1:p.Ile204Thr
NM_001287387.2:c.281T>C	NP_001274316.1:p.Ile94Thr
NR_046298.3:n.514T>C