Canonical Allele Identifier: CA360696919

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097270A>T (hg19) ; chr5:g.110761570A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761570A>T , CM000667.2:g.110761570A>T	GRCh38
NC_000005.9:g.110097270A>T , CM000667.1:g.110097270A>T	GRCh37
NC_000005.8:g.110125169A>T	NCBI36
NG_051334.1:g.28435A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1045A>T MANE Select	ENSP00000348211.3:p.Ile349Leu
ENST00000355943.7:c.1045A>T	ENSP00000348211.3:p.Ile349Leu
ENST00000447245.6:c.802A>T	ENSP00000399717.2:p.Ile268Leu
ENST00000502462.6:n.1361A>T
ENST00000504098.1:c.607A>T	ENSP00000425708.1:p.Ile203Leu
ENST00000509432.1:c.406A>T	ENSP00000426604.1:p.Ile136Leu
ENST00000513706.2:n.2645A>T
ENST00000513807.5:c.559A>T	ENSP00000421134.1:p.Ile187Leu
NM_001303249.1:c.802A>T	NP_001290178.1:p.Ile268Leu
NM_001303250.1:c.772A>T	NP_001290179.1:p.Ile258Leu
NM_138773.2:c.1045A>T	NP_620128.1:p.Ile349Leu
NM_001303249.2:c.802A>T	NP_001290178.1:p.Ile268Leu
NM_001303250.2:c.772A>T	NP_001290179.1:p.Ile258Leu
NM_138773.3:c.1045A>T	NP_620128.1:p.Ile349Leu
NR_138151.1:n.1319A>T
NM_138773.4:c.1045A>T MANE Select	NP_620128.1:p.Ile349Leu
NM_001303249.3:c.802A>T	NP_001290178.1:p.Ile268Leu
NM_001303250.3:c.772A>T	NP_001290179.1:p.Ile258Leu
NR_138151.2:n.1284A>T