Canonical Allele Identifier: CA445802339

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110082005A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110746304A>T , CM000667.2:g.110746304A>T	GRCh38
NC_000005.9:g.110082005A>T , CM000667.1:g.110082005A>T	GRCh37
NC_000005.8:g.110109904A>T	NCBI36
NG_051334.1:g.13169A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355943.8:c.420A>T MANE Select	ENSP00000348211.3:p.Pro140=
ENST00000355943.7:c.420A>T	ENSP00000348211.3:p.Pro140=
ENST00000447245.6:c.420A>T	ENSP00000399717.2:p.Pro140=
ENST00000502462.6:n.736A>T
ENST00000504098.1:c.-19A>T	ENSP00000425708.1:n.-19A>T
ENST00000508781.5:n.249A>T
ENST00000513807.5:c.-67A>T	ENSP00000421134.1:n.-67A>T
NM_001303249.1:c.420A>T	NP_001290178.1:p.Pro140=
NM_001303250.1:c.147A>T	NP_001290179.1:p.Pro49=
NM_138773.2:c.420A>T	NP_620128.1:p.Pro140=
XM_011543708.1:c.420A>T	XP_011542010.1:p.Pro140=
NM_001303249.2:c.420A>T	NP_001290178.1:p.Pro140=
NM_001303250.2:c.147A>T	NP_001290179.1:p.Pro49=
NM_138773.3:c.420A>T	NP_620128.1:p.Pro140=
NR_138151.1:n.568A>T
NM_138773.4:c.420A>T MANE Select	NP_620128.1:p.Pro140=
NM_001303249.3:c.420A>T	NP_001290178.1:p.Pro140=
NM_001303250.3:c.147A>T	NP_001290179.1:p.Pro49=
NR_138151.2:n.533A>T