Canonical Allele Identifier: CA1918678281

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361965G= , CM000672.2:g.71361965G=	GRCh38
NC_000010.10:g.73121722G= , CM000672.1:g.73121722G=	GRCh37
NC_000010.9:g.72791728G=	NCBI36
NG_017066.1:g.47713G=
NG_017066.2:g.47707G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2261G=
ENST00000373189.6:c.785G= MANE Select	ENSP00000362285.5:p.Arg262=
ENST00000479577.2:c.551G=	ENSP00000493995.1:p.Arg184=
ENST00000642198.1:c.*357G=	ENSP00000494827.1:n.*357G=
ENST00000642772.1:c.*94+5722G=	ENSP00000495041.1:n.*94+5722G=
ENST00000643042.1:c.406G=	ENSP00000496674.1:n.406G=
ENST00000643619.1:c.*368G=	ENSP00000494378.1:n.*368G=
ENST00000643752.1:c.*111G=	ENSP00000495000.1:n.*111G=
ENST00000644088.1:c.*106G=	ENSP00000494066.1:n.*106G=
ENST00000644591.1:c.*111G=	ENSP00000496664.1:n.*111G=
ENST00000644895.1:c.*99+5722G=	ENSP00000493872.1:n.*99+5722G=
ENST00000645345.1:c.*357G=	ENSP00000495859.1:n.*357G=
ENST00000647524.1:c.*368G=	ENSP00000495077.1:n.*368G=
ENST00000373189.5:c.785G=	ENSP00000362285.5:p.Arg262=
ENST00000469204.1:n.282G=
NM_001174098.1:c.*14G=	NP_001167569.1:n.*14G=
NM_018344.5:c.785G=	NP_060814.4:p.Arg262=
NR_033413.1:n.759G=
NR_033414.1:n.532G=
XM_006717910.2:c.551G=	XP_006717973.1:p.Arg184=
NM_001363518.1:c.551G=	NP_001350447.1:p.Arg184=
XM_017016377.2:c.347G=	XP_016871866.1:p.Arg116=
XM_017016378.2:c.167G=	XP_016871867.1:p.Arg56=
NM_018344.6:c.785G= MANE Select	NP_060814.4:p.Arg262=
NM_001174098.2:c.*14G=	NP_001167569.1:n.*14G=
NM_001363518.2:c.551G=	NP_001350447.1:p.Arg184=
NR_033413.2:n.753G=
NR_033414.2:n.526G=