Canonical Allele Identifier: CA410637146

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164388A>G (hg19) ; chr22:g.19176875A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176875A>G , CM000684.2:g.19176875A>G	GRCh38
NC_000022.10:g.19164388A>G , CM000684.1:g.19164388A>G	GRCh37
NC_000022.9:g.17544388A>G	NCBI36
NG_033863.1:g.6989T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.602T>C MANE Select	ENSP00000215882.5:p.Val201Ala
ENST00000215882.9:c.602T>C	ENSP00000215882.5:p.Val201Ala
ENST00000451283.5:c.293T>C	ENSP00000401480.1:p.Val98Ala
ENST00000461267.1:n.748T>C
ENST00000470922.5:n.744T>C
NM_001256534.1:c.623T>C	NP_001243463.1:p.Val208Ala
NM_001287387.1:c.293T>C	NP_001274316.1:p.Val98Ala
NM_005984.4:c.602T>C	NP_005975.1:p.Val201Ala
NR_046298.2:n.653T>C
NM_005984.5:c.602T>C MANE Select	NP_005975.1:p.Val201Ala
NM_001256534.2:c.623T>C	NP_001243463.1:p.Val208Ala
NM_001287387.2:c.293T>C	NP_001274316.1:p.Val98Ala
NR_046298.3:n.526T>C