Canonical Allele Identifier: CA410636813

Gene: SLC25A1

Linked Data

• MyVariant Identifiers: chr22:g.19164203T>G (hg19) ; chr22:g.19176690T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176690T>G , CM000684.2:g.19176690T>G	GRCh38
NC_000022.10:g.19164203T>G , CM000684.1:g.19164203T>G	GRCh37
NC_000022.9:g.17544203T>G	NCBI36
NG_033863.1:g.7174A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.635A>C MANE Select	ENSP00000215882.5:p.Asp212Ala
ENST00000215882.9:c.635A>C	ENSP00000215882.5:p.Asp212Ala
ENST00000451283.5:c.326A>C	ENSP00000401480.1:p.Asp109Ala
ENST00000461267.1:n.781A>C
ENST00000470922.5:n.777A>C
NM_001256534.1:c.656A>C	NP_001243463.1:p.Asp219Ala
NM_001287387.1:c.326A>C	NP_001274316.1:p.Asp109Ala
NM_005984.4:c.635A>C	NP_005975.1:p.Asp212Ala
NR_046298.2:n.686A>C
NM_005984.5:c.635A>C MANE Select	NP_005975.1:p.Asp212Ala
NM_001256534.2:c.656A>C	NP_001243463.1:p.Asp219Ala
NM_001287387.2:c.326A>C	NP_001274316.1:p.Asp109Ala
NR_046298.3:n.559A>C