Canonical Allele Identifier: CA2655261570
Gene: SLC25A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19177055A>C , CM000684.2:g.19177055A>C GRCh38
NC_000022.10:g.19164568A>C , CM000684.1:g.19164568A>C GRCh37
NC_000022.9:g.17544568A>C NCBI36
NG_033863.1:g.6809T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215882.10:c.526+65T>G MANE Select ENSP00000215882.5:n.526+65T>G
ENST00000215882.9:c.526+65T>G ENSP00000215882.5:n.526+65T>G
ENST00000451283.5:c.217+65T>G ENSP00000401480.1:n.217+65T>G
ENST00000461267.1:n.672+65T>G
ENST00000470922.5:n.668+65T>G
NM_001256534.1:c.547+65T>G NP_001243463.1:n.547+65T>G
NM_001287387.1:c.217+65T>G NP_001274316.1:n.217+65T>G
NM_005984.4:c.526+65T>G NP_005975.1:n.526+65T>G
NR_046298.2:n.577+65T>G
NM_005984.5:c.526+65T>G MANE Select NP_005975.1:n.526+65T>G
NM_001256534.2:c.547+65T>G NP_001243463.1:n.547+65T>G
NM_001287387.2:c.217+65T>G NP_001274316.1:n.217+65T>G
NR_046298.3:n.450+65T>G