Canonical Allele Identifier: CA360697461

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097356G>T (hg19) ; chr5:g.110761656G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761656G>T , CM000667.2:g.110761656G>T	GRCh38
NC_000005.9:g.110097356G>T , CM000667.1:g.110097356G>T	GRCh37
NC_000005.8:g.110125255G>T	NCBI36
NG_051334.1:g.28521G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1131G>T MANE Select	ENSP00000348211.3:p.Arg377Ser
ENST00000355943.7:c.1131G>T	ENSP00000348211.3:p.Arg377Ser
ENST00000447245.6:c.888G>T	ENSP00000399717.2:p.Arg296Ser
ENST00000504098.1:c.693G>T	ENSP00000425708.1:p.Arg231Ser
ENST00000509432.1:c.492G>T	ENSP00000426604.1:p.Arg164Ser
ENST00000513706.2:n.2731G>T
ENST00000513807.5:c.645G>T	ENSP00000421134.1:p.Arg215Ser
NM_001303249.1:c.888G>T	NP_001290178.1:p.Arg296Ser
NM_001303250.1:c.858G>T	NP_001290179.1:p.Arg286Ser
NM_138773.2:c.1131G>T	NP_620128.1:p.Arg377Ser
NM_001303249.2:c.888G>T	NP_001290178.1:p.Arg296Ser
NM_001303250.2:c.858G>T	NP_001290179.1:p.Arg286Ser
NM_138773.3:c.1131G>T	NP_620128.1:p.Arg377Ser
NR_138151.1:n.1405G>T
NM_138773.4:c.1131G>T MANE Select	NP_620128.1:p.Arg377Ser
NM_001303249.3:c.888G>T	NP_001290178.1:p.Arg296Ser
NM_001303250.3:c.858G>T	NP_001290179.1:p.Arg286Ser
NR_138151.2:n.1370G>T