Canonical Allele Identifier: CA513188092

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164396G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176883G>A , CM000684.2:g.19176883G>A	GRCh38
NC_000022.10:g.19164396G>A , CM000684.1:g.19164396G>A	GRCh37
NC_000022.9:g.17544396G>A	NCBI36
NG_033863.1:g.6981C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.594C>T MANE Select	ENSP00000215882.5:p.Arg198=
ENST00000215882.9:c.594C>T	ENSP00000215882.5:p.Arg198=
ENST00000451283.5:c.285C>T	ENSP00000401480.1:p.Arg95=
ENST00000461267.1:n.740C>T
ENST00000470922.5:n.736C>T
NM_001256534.1:c.615C>T	NP_001243463.1:p.Arg205=
NM_001287387.1:c.285C>T	NP_001274316.1:p.Arg95=
NM_005984.4:c.594C>T	NP_005975.1:p.Arg198=
NR_046298.2:n.645C>T
NM_005984.5:c.594C>T MANE Select	NP_005975.1:p.Arg198=
NM_001256534.2:c.615C>T	NP_001243463.1:p.Arg205=
NM_001287387.2:c.285C>T	NP_001274316.1:p.Arg95=
NR_046298.3:n.518C>T