Canonical Allele Identifier: CA2577643134
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177660G>C , CM000684.2:g.19177660G>C GRCh38
NC_000022.10:g.19165173G>C , CM000684.1:g.19165173G>C GRCh37
NC_000022.9:g.17545173G>C NCBI36
NG_033805.1:g.119057C>G
NG_033863.1:g.6204C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.441+67C>G MANE Select ENSP00000215882.5:n.441+67C>G
ENST00000215882.9:c.441+67C>G ENSP00000215882.5:n.441+67C>G
ENST00000451283.5:c.132+67C>G ENSP00000401480.1:n.132+67C>G
ENST00000461267.1:n.587+67C>G
ENST00000470922.5:n.583+67C>G
NM_001256534.1:c.462+67C>G NP_001243463.1:n.462+67C>G
NM_001287387.1:c.132+67C>G NP_001274316.1:n.132+67C>G
NM_005984.4:c.441+67C>G NP_005975.1:n.441+67C>G
NR_046298.2:n.492+282C>G
NM_005984.5:c.441+67C>G MANE Select NP_005975.1:n.441+67C>G
NM_001256534.2:c.462+67C>G NP_001243463.1:n.462+67C>G
NM_001287387.2:c.132+67C>G NP_001274316.1:n.132+67C>G
NR_046298.3:n.365+282C>G