Canonical Allele Identifier: CA445803848

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110096933T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761233T>A , CM000667.2:g.110761233T>A	GRCh38
NC_000005.9:g.110096933T>A , CM000667.1:g.110096933T>A	GRCh37
NC_000005.8:g.110124832T>A	NCBI36
NG_051334.1:g.28098T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.708T>A MANE Select	ENSP00000348211.3:p.Ile236=
ENST00000355943.7:c.708T>A	ENSP00000348211.3:p.Ile236=
ENST00000447245.6:c.679-214T>A	ENSP00000399717.2:n.679-214T>A
ENST00000502462.6:n.1024T>A
ENST00000504098.1:c.270T>A	ENSP00000425708.1:p.Ile90=
ENST00000509432.1:c.69T>A	ENSP00000426604.1:p.Ile23=
ENST00000513706.2:n.2308T>A
ENST00000513807.5:c.222T>A	ENSP00000421134.1:p.Ile74=
NM_001303249.1:c.679-214T>A	NP_001290178.1:n.679-214T>A
NM_001303250.1:c.435T>A	NP_001290179.1:p.Ile145=
NM_138773.2:c.708T>A	NP_620128.1:p.Ile236=
NM_001303249.2:c.679-214T>A	NP_001290178.1:n.679-214T>A
NM_001303250.2:c.435T>A	NP_001290179.1:p.Ile145=
NM_138773.3:c.708T>A	NP_620128.1:p.Ile236=
NR_138151.1:n.982T>A
NM_138773.4:c.708T>A MANE Select	NP_620128.1:p.Ile236=
NM_001303249.3:c.679-214T>A	NP_001290178.1:n.679-214T>A
NM_001303250.3:c.435T>A	NP_001290179.1:p.Ile145=
NR_138151.2:n.947T>A