Canonical Allele Identifier: CA360697422

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097349C>G (hg19) ; chr5:g.110761649C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761649C>G , CM000667.2:g.110761649C>G	GRCh38
NC_000005.9:g.110097349C>G , CM000667.1:g.110097349C>G	GRCh37
NC_000005.8:g.110125248C>G	NCBI36
NG_051334.1:g.28514C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1124C>G MANE Select	ENSP00000348211.3:p.Thr375Ser
ENST00000355943.7:c.1124C>G	ENSP00000348211.3:p.Thr375Ser
ENST00000447245.6:c.881C>G	ENSP00000399717.2:p.Thr294Ser
ENST00000502462.6:n.1440C>G
ENST00000504098.1:c.686C>G	ENSP00000425708.1:p.Thr229Ser
ENST00000509432.1:c.485C>G	ENSP00000426604.1:p.Thr162Ser
ENST00000513706.2:n.2724C>G
ENST00000513807.5:c.638C>G	ENSP00000421134.1:p.Thr213Ser
NM_001303249.1:c.881C>G	NP_001290178.1:p.Thr294Ser
NM_001303250.1:c.851C>G	NP_001290179.1:p.Thr284Ser
NM_138773.2:c.1124C>G	NP_620128.1:p.Thr375Ser
NM_001303249.2:c.881C>G	NP_001290178.1:p.Thr294Ser
NM_001303250.2:c.851C>G	NP_001290179.1:p.Thr284Ser
NM_138773.3:c.1124C>G	NP_620128.1:p.Thr375Ser
NR_138151.1:n.1398C>G
NM_138773.4:c.1124C>G MANE Select	NP_620128.1:p.Thr375Ser
NM_001303249.3:c.881C>G	NP_001290178.1:p.Thr294Ser
NM_001303250.3:c.851C>G	NP_001290179.1:p.Thr284Ser
NR_138151.2:n.1363C>G