Canonical Allele Identifier: CA2395758732

Gene: SLC25A1

Linked Data

• dbSNP Id: rs2083982714
• gnomAD v4: 22-19177626-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177626C>A , CM000684.2:g.19177626C>A	GRCh38
NC_000022.10:g.19165139C>A , CM000684.1:g.19165139C>A	GRCh37
NC_000022.9:g.17545139C>A	NCBI36
NG_033805.1:g.119091G>T
NG_033863.1:g.6238G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.441+101G>T MANE Select	ENSP00000215882.5:n.441+101G>T
ENST00000215882.9:c.441+101G>T	ENSP00000215882.5:n.441+101G>T
ENST00000451283.5:c.132+101G>T	ENSP00000401480.1:n.132+101G>T
ENST00000461267.1:n.587+101G>T
ENST00000470922.5:n.583+101G>T
NM_001256534.1:c.462+101G>T	NP_001243463.1:n.462+101G>T
NM_001287387.1:c.132+101G>T	NP_001274316.1:n.132+101G>T
NM_005984.4:c.441+101G>T	NP_005975.1:n.441+101G>T
NR_046298.2:n.492+316G>T
NM_005984.5:c.441+101G>T MANE Select	NP_005975.1:n.441+101G>T
NM_001256534.2:c.462+101G>T	NP_001243463.1:n.462+101G>T
NM_001287387.2:c.132+101G>T	NP_001274316.1:n.132+101G>T
NR_046298.3:n.365+316G>T