Canonical Allele Identifier: CA1918678292

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361981C= , CM000672.2:g.71361981C=	GRCh38
NC_000010.10:g.73121738C= , CM000672.1:g.73121738C=	GRCh37
NC_000010.9:g.72791744C=	NCBI36
NG_017066.1:g.47729C=
NG_017066.2:g.47723C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2277C=
ENST00000373189.6:c.801C= MANE Select	ENSP00000362285.5:p.Ala267=
ENST00000479577.2:c.567C=	ENSP00000493995.1:p.Ala189=
ENST00000642198.1:c.*373C=	ENSP00000494827.1:n.*373C=
ENST00000642772.1:c.*94+5738C=	ENSP00000495041.1:n.*94+5738C=
ENST00000643042.1:c.422C=	ENSP00000496674.1:n.422C=
ENST00000643619.1:c.*384C=	ENSP00000494378.1:n.*384C=
ENST00000643752.1:c.*127C=	ENSP00000495000.1:n.*127C=
ENST00000644088.1:c.*122C=	ENSP00000494066.1:n.*122C=
ENST00000644591.1:c.*127C=	ENSP00000496664.1:n.*127C=
ENST00000644895.1:c.*99+5738C=	ENSP00000493872.1:n.*99+5738C=
ENST00000645345.1:c.*373C=	ENSP00000495859.1:n.*373C=
ENST00000647524.1:c.*384C=	ENSP00000495077.1:n.*384C=
ENST00000373189.5:c.801C=	ENSP00000362285.5:p.Ala267=
ENST00000469204.1:n.298C=
NM_001174098.1:c.*30C=	NP_001167569.1:n.*30C=
NM_018344.5:c.801C=	NP_060814.4:p.Ala267=
NR_033413.1:n.775C=
NR_033414.1:n.548C=
XM_006717910.2:c.567C=	XP_006717973.1:p.Ala189=
NM_001363518.1:c.567C=	NP_001350447.1:p.Ala189=
XM_017016377.2:c.363C=	XP_016871866.1:p.Ala121=
XM_017016378.2:c.183C=	XP_016871867.1:p.Ala61=
NM_018344.6:c.801C= MANE Select	NP_060814.4:p.Ala267=
NM_001174098.2:c.*30C=	NP_001167569.1:n.*30C=
NM_001363518.2:c.567C=	NP_001350447.1:p.Ala189=
NR_033413.2:n.769C=
NR_033414.2:n.542C=