Canonical Allele Identifier: CA2395758384

Gene: SLC25A1

Linked Data

• dbSNP Id: rs1601398500
• gnomAD v4: 22-19176761-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176761T>G , CM000684.2:g.19176761T>G	GRCh38
NC_000022.10:g.19164274T>G , CM000684.1:g.19164274T>G	GRCh37
NC_000022.9:g.17544274T>G	NCBI36
NG_033863.1:g.7103A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.632-68A>C MANE Select	ENSP00000215882.5:n.632-68A>C
ENST00000215882.9:c.632-68A>C	ENSP00000215882.5:n.632-68A>C
ENST00000451283.5:c.323-68A>C	ENSP00000401480.1:n.323-68A>C
ENST00000461267.1:n.778-68A>C
ENST00000470922.5:n.774-68A>C
NM_001256534.1:c.653-68A>C	NP_001243463.1:n.653-68A>C
NM_001287387.1:c.323-68A>C	NP_001274316.1:n.323-68A>C
NM_005984.4:c.632-68A>C	NP_005975.1:n.632-68A>C
NR_046298.2:n.683-68A>C
NM_005984.5:c.632-68A>C MANE Select	NP_005975.1:n.632-68A>C
NM_001256534.2:c.653-68A>C	NP_001243463.1:n.653-68A>C
NM_001287387.2:c.323-68A>C	NP_001274316.1:n.323-68A>C
NR_046298.3:n.556-68A>C