Canonical Allele Identifier: CA445964574

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097350C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761650C>A , CM000667.2:g.110761650C>A	GRCh38
NC_000005.9:g.110097350C>A , CM000667.1:g.110097350C>A	GRCh37
NC_000005.8:g.110125249C>A	NCBI36
NG_051334.1:g.28515C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1125C>A MANE Select	ENSP00000348211.3:p.Thr375=
ENST00000355943.7:c.1125C>A	ENSP00000348211.3:p.Thr375=
ENST00000447245.6:c.882C>A	ENSP00000399717.2:p.Thr294=
ENST00000502462.6:n.1441C>A
ENST00000504098.1:c.687C>A	ENSP00000425708.1:p.Thr229=
ENST00000509432.1:c.486C>A	ENSP00000426604.1:p.Thr162=
ENST00000513706.2:n.2725C>A
ENST00000513807.5:c.639C>A	ENSP00000421134.1:p.Thr213=
NM_001303249.1:c.882C>A	NP_001290178.1:p.Thr294=
NM_001303250.1:c.852C>A	NP_001290179.1:p.Thr284=
NM_138773.2:c.1125C>A	NP_620128.1:p.Thr375=
NM_001303249.2:c.882C>A	NP_001290178.1:p.Thr294=
NM_001303250.2:c.852C>A	NP_001290179.1:p.Thr284=
NM_138773.3:c.1125C>A	NP_620128.1:p.Thr375=
NR_138151.1:n.1399C>A
NM_138773.4:c.1125C>A MANE Select	NP_620128.1:p.Thr375=
NM_001303249.3:c.882C>A	NP_001290178.1:p.Thr294=
NM_001303250.3:c.852C>A	NP_001290179.1:p.Thr284=
NR_138151.2:n.1364C>A