Canonical Allele Identifier: CA360697390

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097344C>G (hg19) ; chr5:g.110761644C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761644C>G , CM000667.2:g.110761644C>G	GRCh38
NC_000005.9:g.110097344C>G , CM000667.1:g.110097344C>G	GRCh37
NC_000005.8:g.110125243C>G	NCBI36
NG_051334.1:g.28509C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1119C>G MANE Select	ENSP00000348211.3:p.Ile373Met
ENST00000355943.7:c.1119C>G	ENSP00000348211.3:p.Ile373Met
ENST00000447245.6:c.876C>G	ENSP00000399717.2:p.Ile292Met
ENST00000502462.6:n.1435C>G
ENST00000504098.1:c.681C>G	ENSP00000425708.1:p.Ile227Met
ENST00000509432.1:c.480C>G	ENSP00000426604.1:p.Ile160Met
ENST00000513706.2:n.2719C>G
ENST00000513807.5:c.633C>G	ENSP00000421134.1:p.Ile211Met
NM_001303249.1:c.876C>G	NP_001290178.1:p.Ile292Met
NM_001303250.1:c.846C>G	NP_001290179.1:p.Ile282Met
NM_138773.2:c.1119C>G	NP_620128.1:p.Ile373Met
NM_001303249.2:c.876C>G	NP_001290178.1:p.Ile292Met
NM_001303250.2:c.846C>G	NP_001290179.1:p.Ile282Met
NM_138773.3:c.1119C>G	NP_620128.1:p.Ile373Met
NR_138151.1:n.1393C>G
NM_138773.4:c.1119C>G MANE Select	NP_620128.1:p.Ile373Met
NM_001303249.3:c.876C>G	NP_001290178.1:p.Ile292Met
NM_001303250.3:c.846C>G	NP_001290179.1:p.Ile282Met
NR_138151.2:n.1358C>G