Canonical Allele Identifier: CA2395758568

Gene: SLC25A1

Linked Data

• dbSNP Id: rs1555922587
• gnomAD v4: 22-19177064-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177064C>G , CM000684.2:g.19177064C>G	GRCh38
NC_000022.10:g.19164577C>G , CM000684.1:g.19164577C>G	GRCh37
NC_000022.9:g.17544577C>G	NCBI36
NG_033863.1:g.6800G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.526+56G>C MANE Select	ENSP00000215882.5:n.526+56G>C
ENST00000215882.9:c.526+56G>C	ENSP00000215882.5:n.526+56G>C
ENST00000451283.5:c.217+56G>C	ENSP00000401480.1:n.217+56G>C
ENST00000461267.1:n.672+56G>C
ENST00000470922.5:n.668+56G>C
NM_001256534.1:c.547+56G>C	NP_001243463.1:n.547+56G>C
NM_001287387.1:c.217+56G>C	NP_001274316.1:n.217+56G>C
NM_005984.4:c.526+56G>C	NP_005975.1:n.526+56G>C
NR_046298.2:n.577+56G>C
NM_005984.5:c.526+56G>C MANE Select	NP_005975.1:n.526+56G>C
NM_001256534.2:c.547+56G>C	NP_001243463.1:n.547+56G>C
NM_001287387.2:c.217+56G>C	NP_001274316.1:n.217+56G>C
NR_046298.3:n.450+56G>C