Canonical Allele Identifier: CA445964732

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097479T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761779T>A , CM000667.2:g.110761779T>A	GRCh38
NC_000005.9:g.110097479T>A , CM000667.1:g.110097479T>A	GRCh37
NC_000005.8:g.110125378T>A	NCBI36
NG_051334.1:g.28644T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1254T>A MANE Select	ENSP00000348211.3:p.Ile418=
ENST00000355943.7:c.1254T>A	ENSP00000348211.3:p.Ile418=
ENST00000447245.6:c.1011T>A	ENSP00000399717.2:p.Ile337=
ENST00000504098.1:c.816T>A	ENSP00000425708.1:p.Ile272=
ENST00000509432.1:c.615T>A	ENSP00000426604.1:p.Ile205=
ENST00000513706.2:n.2854T>A
ENST00000513807.5:c.768T>A	ENSP00000421134.1:p.Ile256=
NM_001303249.1:c.1011T>A	NP_001290178.1:p.Ile337=
NM_001303250.1:c.981T>A	NP_001290179.1:p.Ile327=
NM_138773.2:c.1254T>A	NP_620128.1:p.Ile418=
NM_001303249.2:c.1011T>A	NP_001290178.1:p.Ile337=
NM_001303250.2:c.981T>A	NP_001290179.1:p.Ile327=
NM_138773.3:c.1254T>A	NP_620128.1:p.Ile418=
NR_138151.1:n.1528T>A
NM_138773.4:c.1254T>A MANE Select	NP_620128.1:p.Ile418=
NM_001303249.3:c.1011T>A	NP_001290178.1:p.Ile337=
NM_001303250.3:c.981T>A	NP_001290179.1:p.Ile327=
NR_138151.2:n.1493T>A