Canonical Allele Identifier: CA360697143

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097307C>A (hg19) ; chr5:g.110761607C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761607C>A , CM000667.2:g.110761607C>A	GRCh38
NC_000005.9:g.110097307C>A , CM000667.1:g.110097307C>A	GRCh37
NC_000005.8:g.110125206C>A	NCBI36
NG_051334.1:g.28472C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1082C>A MANE Select	ENSP00000348211.3:p.Pro361Gln
ENST00000355943.7:c.1082C>A	ENSP00000348211.3:p.Pro361Gln
ENST00000447245.6:c.839C>A	ENSP00000399717.2:p.Pro280Gln
ENST00000502462.6:n.1398C>A
ENST00000504098.1:c.644C>A	ENSP00000425708.1:p.Pro215Gln
ENST00000509432.1:c.443C>A	ENSP00000426604.1:p.Pro148Gln
ENST00000513706.2:n.2682C>A
ENST00000513807.5:c.596C>A	ENSP00000421134.1:p.Pro199Gln
NM_001303249.1:c.839C>A	NP_001290178.1:p.Pro280Gln
NM_001303250.1:c.809C>A	NP_001290179.1:p.Pro270Gln
NM_138773.2:c.1082C>A	NP_620128.1:p.Pro361Gln
NM_001303249.2:c.839C>A	NP_001290178.1:p.Pro280Gln
NM_001303250.2:c.809C>A	NP_001290179.1:p.Pro270Gln
NM_138773.3:c.1082C>A	NP_620128.1:p.Pro361Gln
NR_138151.1:n.1356C>A
NM_138773.4:c.1082C>A MANE Select	NP_620128.1:p.Pro361Gln
NM_001303249.3:c.839C>A	NP_001290178.1:p.Pro280Gln
NM_001303250.3:c.809C>A	NP_001290179.1:p.Pro270Gln
NR_138151.2:n.1321C>A