Canonical Allele Identifier: CA445964651

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097416A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761716A>T , CM000667.2:g.110761716A>T	GRCh38
NC_000005.9:g.110097416A>T , CM000667.1:g.110097416A>T	GRCh37
NC_000005.8:g.110125315A>T	NCBI36
NG_051334.1:g.28581A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1191A>T MANE Select	ENSP00000348211.3:p.Thr397=
ENST00000355943.7:c.1191A>T	ENSP00000348211.3:p.Thr397=
ENST00000447245.6:c.948A>T	ENSP00000399717.2:p.Thr316=
ENST00000504098.1:c.753A>T	ENSP00000425708.1:p.Thr251=
ENST00000509432.1:c.552A>T	ENSP00000426604.1:p.Thr184=
ENST00000513706.2:n.2791A>T
ENST00000513807.5:c.705A>T	ENSP00000421134.1:p.Thr235=
NM_001303249.1:c.948A>T	NP_001290178.1:p.Thr316=
NM_001303250.1:c.918A>T	NP_001290179.1:p.Thr306=
NM_138773.2:c.1191A>T	NP_620128.1:p.Thr397=
NM_001303249.2:c.948A>T	NP_001290178.1:p.Thr316=
NM_001303250.2:c.918A>T	NP_001290179.1:p.Thr306=
NM_138773.3:c.1191A>T	NP_620128.1:p.Thr397=
NR_138151.1:n.1465A>T
NM_138773.4:c.1191A>T MANE Select	NP_620128.1:p.Thr397=
NM_001303249.3:c.948A>T	NP_001290178.1:p.Thr316=
NM_001303250.3:c.918A>T	NP_001290179.1:p.Thr306=
NR_138151.2:n.1430A>T