Canonical Allele Identifier: CA1572423628

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761447A= , CM000667.2:g.110761447A=	GRCh38
NC_000005.9:g.110097147A= , CM000667.1:g.110097147A=	GRCh37
NC_000005.8:g.110125046A=	NCBI36
NG_051334.1:g.28312A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355943.8:c.922A= MANE Select	ENSP00000348211.3:p.Ser308=
ENST00000355943.7:c.922A=	ENSP00000348211.3:p.Ser308=
ENST00000447245.6:c.679A=	ENSP00000399717.2:p.Ser227=
ENST00000502462.6:n.1238A=
ENST00000504098.1:c.484A=	ENSP00000425708.1:p.Ser162=
ENST00000509432.1:c.283A=	ENSP00000426604.1:p.Ser95=
ENST00000513706.2:n.2522A=
ENST00000513807.5:c.436A=	ENSP00000421134.1:p.Ser146=
NM_001303249.1:c.679A=	NP_001290178.1:p.Ser227=
NM_001303250.1:c.649A=	NP_001290179.1:p.Ser217=
NM_138773.2:c.922A=	NP_620128.1:p.Ser308=
NM_001303249.2:c.679A=	NP_001290178.1:p.Ser227=
NM_001303250.2:c.649A=	NP_001290179.1:p.Ser217=
NM_138773.3:c.922A=	NP_620128.1:p.Ser308=
NR_138151.1:n.1196A=
NM_138773.4:c.922A= MANE Select	NP_620128.1:p.Ser308=
NM_001303249.3:c.679A=	NP_001290178.1:p.Ser227=
NM_001303250.3:c.649A=	NP_001290179.1:p.Ser217=
NR_138151.2:n.1161A=