Canonical Allele Identifier: CA445964620

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097395T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761695T>C , CM000667.2:g.110761695T>C	GRCh38
NC_000005.9:g.110097395T>C , CM000667.1:g.110097395T>C	GRCh37
NC_000005.8:g.110125294T>C	NCBI36
NG_051334.1:g.28560T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1170T>C MANE Select	ENSP00000348211.3:p.Gly390=
ENST00000355943.7:c.1170T>C	ENSP00000348211.3:p.Gly390=
ENST00000447245.6:c.927T>C	ENSP00000399717.2:p.Gly309=
ENST00000504098.1:c.732T>C	ENSP00000425708.1:p.Gly244=
ENST00000509432.1:c.531T>C	ENSP00000426604.1:p.Gly177=
ENST00000513706.2:n.2770T>C
ENST00000513807.5:c.684T>C	ENSP00000421134.1:p.Gly228=
NM_001303249.1:c.927T>C	NP_001290178.1:p.Gly309=
NM_001303250.1:c.897T>C	NP_001290179.1:p.Gly299=
NM_138773.2:c.1170T>C	NP_620128.1:p.Gly390=
NM_001303249.2:c.927T>C	NP_001290178.1:p.Gly309=
NM_001303250.2:c.897T>C	NP_001290179.1:p.Gly299=
NM_138773.3:c.1170T>C	NP_620128.1:p.Gly390=
NR_138151.1:n.1444T>C
NM_138773.4:c.1170T>C MANE Select	NP_620128.1:p.Gly390=
NM_001303249.3:c.927T>C	NP_001290178.1:p.Gly309=
NM_001303250.3:c.897T>C	NP_001290179.1:p.Gly299=
NR_138151.2:n.1409T>C