Canonical Allele Identifier: CA445964628

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097398T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761698T>G , CM000667.2:g.110761698T>G	GRCh38
NC_000005.9:g.110097398T>G , CM000667.1:g.110097398T>G	GRCh37
NC_000005.8:g.110125297T>G	NCBI36
NG_051334.1:g.28563T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1173T>G MANE Select	ENSP00000348211.3:p.Ala391=
ENST00000355943.7:c.1173T>G	ENSP00000348211.3:p.Ala391=
ENST00000447245.6:c.930T>G	ENSP00000399717.2:p.Ala310=
ENST00000504098.1:c.735T>G	ENSP00000425708.1:p.Ala245=
ENST00000509432.1:c.534T>G	ENSP00000426604.1:p.Ala178=
ENST00000513706.2:n.2773T>G
ENST00000513807.5:c.687T>G	ENSP00000421134.1:p.Ala229=
NM_001303249.1:c.930T>G	NP_001290178.1:p.Ala310=
NM_001303250.1:c.900T>G	NP_001290179.1:p.Ala300=
NM_138773.2:c.1173T>G	NP_620128.1:p.Ala391=
NM_001303249.2:c.930T>G	NP_001290178.1:p.Ala310=
NM_001303250.2:c.900T>G	NP_001290179.1:p.Ala300=
NM_138773.3:c.1173T>G	NP_620128.1:p.Ala391=
NR_138151.1:n.1447T>G
NM_138773.4:c.1173T>G MANE Select	NP_620128.1:p.Ala391=
NM_001303249.3:c.930T>G	NP_001290178.1:p.Ala310=
NM_001303250.3:c.900T>G	NP_001290179.1:p.Ala300=
NR_138151.2:n.1412T>G