Canonical Allele Identifier: CA360696486

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097148G>C (hg19) ; chr5:g.110761448G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761448G>C , CM000667.2:g.110761448G>C	GRCh38
NC_000005.9:g.110097148G>C , CM000667.1:g.110097148G>C	GRCh37
NC_000005.8:g.110125047G>C	NCBI36
NG_051334.1:g.28313G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355943.8:c.923G>C MANE Select	ENSP00000348211.3:p.Ser308Thr
ENST00000355943.7:c.923G>C	ENSP00000348211.3:p.Ser308Thr
ENST00000447245.6:c.680G>C	ENSP00000399717.2:p.Ser227Thr
ENST00000502462.6:n.1239G>C
ENST00000504098.1:c.485G>C	ENSP00000425708.1:p.Ser162Thr
ENST00000509432.1:c.284G>C	ENSP00000426604.1:p.Ser95Thr
ENST00000513706.2:n.2523G>C
ENST00000513807.5:c.437G>C	ENSP00000421134.1:p.Ser146Thr
NM_001303249.1:c.680G>C	NP_001290178.1:p.Ser227Thr
NM_001303250.1:c.650G>C	NP_001290179.1:p.Ser217Thr
NM_138773.2:c.923G>C	NP_620128.1:p.Ser308Thr
NM_001303249.2:c.680G>C	NP_001290178.1:p.Ser227Thr
NM_001303250.2:c.650G>C	NP_001290179.1:p.Ser217Thr
NM_138773.3:c.923G>C	NP_620128.1:p.Ser308Thr
NR_138151.1:n.1197G>C
NM_138773.4:c.923G>C MANE Select	NP_620128.1:p.Ser308Thr
NM_001303249.3:c.680G>C	NP_001290178.1:p.Ser227Thr
NM_001303250.3:c.650G>C	NP_001290179.1:p.Ser217Thr
NR_138151.2:n.1162G>C