Canonical Allele Identifier: CA1918678353

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362112G= , CM000672.2:g.71362112G=	GRCh38
NC_000010.10:g.73121869G= , CM000672.1:g.73121869G=	GRCh37
NC_000010.9:g.72791875G=	NCBI36
NG_017066.1:g.47860G=
NG_017066.2:g.47854G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2408G=
ENST00000373189.6:c.932G= MANE Select	ENSP00000362285.5:p.Cys311=
ENST00000479577.2:c.698G=	ENSP00000493995.1:p.Cys233=
ENST00000642198.1:c.*504G=	ENSP00000494827.1:n.*504G=
ENST00000642772.1:c.*94+5869G=	ENSP00000495041.1:n.*94+5869G=
ENST00000643042.1:c.553G=	ENSP00000496674.1:n.553G=
ENST00000643619.1:c.*515G=	ENSP00000494378.1:n.*515G=
ENST00000643752.1:c.*258G=	ENSP00000495000.1:n.*258G=
ENST00000644088.1:c.*253G=	ENSP00000494066.1:n.*253G=
ENST00000644591.1:c.*258G=	ENSP00000496664.1:n.*258G=
ENST00000644895.1:c.*99+5869G=	ENSP00000493872.1:n.*99+5869G=
ENST00000645345.1:c.*504G=	ENSP00000495859.1:n.*504G=
ENST00000647524.1:c.*515G=	ENSP00000495077.1:n.*515G=
ENST00000373189.5:c.932G=	ENSP00000362285.5:p.Cys311=
ENST00000469204.1:n.429G=
NM_001174098.1:c.*161G=	NP_001167569.1:n.*161G=
NM_018344.5:c.932G=	NP_060814.4:p.Cys311=
NR_033413.1:n.906G=
NR_033414.1:n.679G=
XM_006717910.2:c.698G=	XP_006717973.1:p.Cys233=
NM_001363518.1:c.698G=	NP_001350447.1:p.Cys233=
XM_017016377.2:c.494G=	XP_016871866.1:p.Cys165=
XM_017016378.2:c.314G=	XP_016871867.1:p.Cys105=
NM_018344.6:c.932G= MANE Select	NP_060814.4:p.Cys311=
NM_001174098.2:c.*161G=	NP_001167569.1:n.*161G=
NM_001363518.2:c.698G=	NP_001350447.1:p.Cys233=
NR_033413.2:n.900G=
NR_033414.2:n.673G=