Canonical Allele Identifier: CA410636136

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164125T>G (hg19) ; chr22:g.19176612T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176612T>G , CM000684.2:g.19176612T>G	GRCh38
NC_000022.10:g.19164125T>G , CM000684.1:g.19164125T>G	GRCh37
NC_000022.9:g.17544125T>G	NCBI36
NG_033863.1:g.7252A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.713A>C MANE Select	ENSP00000215882.5:p.Asn238Thr
ENST00000215882.9:c.713A>C	ENSP00000215882.5:p.Asn238Thr
ENST00000451283.5:c.404A>C	ENSP00000401480.1:p.Asn135Thr
ENST00000470922.5:n.855A>C
NM_001256534.1:c.734A>C	NP_001243463.1:p.Asn245Thr
NM_001287387.1:c.404A>C	NP_001274316.1:p.Asn135Thr
NM_005984.4:c.713A>C	NP_005975.1:p.Asn238Thr
NR_046298.2:n.764A>C
NM_005984.5:c.713A>C MANE Select	NP_005975.1:p.Asn238Thr
NM_001256534.2:c.734A>C	NP_001243463.1:p.Asn245Thr
NM_001287387.2:c.404A>C	NP_001274316.1:p.Asn135Thr
NR_046298.3:n.637A>C