Canonical Allele Identifier: CA445964774

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097308A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761608A>T , CM000667.2:g.110761608A>T	GRCh38
NC_000005.9:g.110097308A>T , CM000667.1:g.110097308A>T	GRCh37
NC_000005.8:g.110125207A>T	NCBI36
NG_051334.1:g.28473A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1083A>T MANE Select	ENSP00000348211.3:p.Pro361=
ENST00000355943.7:c.1083A>T	ENSP00000348211.3:p.Pro361=
ENST00000447245.6:c.840A>T	ENSP00000399717.2:p.Pro280=
ENST00000502462.6:n.1399A>T
ENST00000504098.1:c.645A>T	ENSP00000425708.1:p.Pro215=
ENST00000509432.1:c.444A>T	ENSP00000426604.1:p.Pro148=
ENST00000513706.2:n.2683A>T
ENST00000513807.5:c.597A>T	ENSP00000421134.1:p.Pro199=
NM_001303249.1:c.840A>T	NP_001290178.1:p.Pro280=
NM_001303250.1:c.810A>T	NP_001290179.1:p.Pro270=
NM_138773.2:c.1083A>T	NP_620128.1:p.Pro361=
NM_001303249.2:c.840A>T	NP_001290178.1:p.Pro280=
NM_001303250.2:c.810A>T	NP_001290179.1:p.Pro270=
NM_138773.3:c.1083A>T	NP_620128.1:p.Pro361=
NR_138151.1:n.1357A>T
NM_138773.4:c.1083A>T MANE Select	NP_620128.1:p.Pro361=
NM_001303249.3:c.840A>T	NP_001290178.1:p.Pro280=
NM_001303250.3:c.810A>T	NP_001290179.1:p.Pro270=
NR_138151.2:n.1322A>T