Canonical Allele Identifier: CA657691017

Gene: SLC25A1

Linked Data

• COSMIC: COSN26537866

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176128G>T , CM000684.2:g.19176128G>T	GRCh38
NC_000022.10:g.19163641G>T , CM000684.1:g.19163641G>T	GRCh37
NC_000022.9:g.17543641G>T	NCBI36
NG_033863.1:g.7736C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.*2C>A MANE Select	ENSP00000215882.5:n.*2C>A
ENST00000215882.9:c.*2C>A	ENSP00000215882.5:n.*2C>A
ENST00000451283.5:c.*2C>A	ENSP00000401480.1:n.*2C>A
ENST00000470922.5:n.1080C>A
NM_001256534.1:c.*2C>A	NP_001243463.1:n.*2C>A
NM_001287387.1:c.*2C>A	NP_001274316.1:n.*2C>A
NM_005984.4:c.*2C>A	NP_005975.1:n.*2C>A
NR_046298.2:n.989C>A
NM_005984.5:c.*2C>A MANE Select	NP_005975.1:n.*2C>A
NM_001256534.2:c.*2C>A	NP_001243463.1:n.*2C>A
NM_001287387.2:c.*2C>A	NP_001274316.1:n.*2C>A
NR_046298.3:n.862C>A