Canonical Allele Identifier: CA2395758562

Gene: SLC25A1

Linked Data

• dbSNP Id: rs2083972713
• gnomAD v4: 22-19177054-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177054G>C , CM000684.2:g.19177054G>C	GRCh38
NC_000022.10:g.19164567G>C , CM000684.1:g.19164567G>C	GRCh37
NC_000022.9:g.17544567G>C	NCBI36
NG_033863.1:g.6810C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.526+66C>G MANE Select	ENSP00000215882.5:n.526+66C>G
ENST00000215882.9:c.526+66C>G	ENSP00000215882.5:n.526+66C>G
ENST00000451283.5:c.217+66C>G	ENSP00000401480.1:n.217+66C>G
ENST00000461267.1:n.672+66C>G
ENST00000470922.5:n.668+66C>G
NM_001256534.1:c.547+66C>G	NP_001243463.1:n.547+66C>G
NM_001287387.1:c.217+66C>G	NP_001274316.1:n.217+66C>G
NM_005984.4:c.526+66C>G	NP_005975.1:n.526+66C>G
NR_046298.2:n.577+66C>G
NM_005984.5:c.526+66C>G MANE Select	NP_005975.1:n.526+66C>G
NM_001256534.2:c.547+66C>G	NP_001243463.1:n.547+66C>G
NM_001287387.2:c.217+66C>G	NP_001274316.1:n.217+66C>G
NR_046298.3:n.450+66C>G