Canonical Allele Identifier: CA2655261575

Gene: SLC25A1

Linked Data

• gnomAD v4: 22-19177061-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177061A>G , CM000684.2:g.19177061A>G	GRCh38
NC_000022.10:g.19164574A>G , CM000684.1:g.19164574A>G	GRCh37
NC_000022.9:g.17544574A>G	NCBI36
NG_033863.1:g.6803T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.526+59T>C MANE Select	ENSP00000215882.5:n.526+59T>C
ENST00000215882.9:c.526+59T>C	ENSP00000215882.5:n.526+59T>C
ENST00000451283.5:c.217+59T>C	ENSP00000401480.1:n.217+59T>C
ENST00000461267.1:n.672+59T>C
ENST00000470922.5:n.668+59T>C
NM_001256534.1:c.547+59T>C	NP_001243463.1:n.547+59T>C
NM_001287387.1:c.217+59T>C	NP_001274316.1:n.217+59T>C
NM_005984.4:c.526+59T>C	NP_005975.1:n.526+59T>C
NR_046298.2:n.577+59T>C
NM_005984.5:c.526+59T>C MANE Select	NP_005975.1:n.526+59T>C
NM_001256534.2:c.547+59T>C	NP_001243463.1:n.547+59T>C
NM_001287387.2:c.217+59T>C	NP_001274316.1:n.217+59T>C
NR_046298.3:n.450+59T>C