Canonical Allele Identifier: CA1918678527

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362477G= , CM000672.2:g.71362477G=	GRCh38
NC_000010.10:g.73122234G= , CM000672.1:g.73122234G=	GRCh37
NC_000010.9:g.72792240G=	NCBI36
NG_017066.1:g.48225G=
NG_017066.2:g.48219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2773G=
ENST00000373189.6:c.1297G= MANE Select	ENSP00000362285.5:p.Ala433=
ENST00000479577.2:c.1063G=	ENSP00000493995.1:p.Ala355=
ENST00000642198.1:c.*869G=	ENSP00000494827.1:n.*869G=
ENST00000642772.1:c.*94+6234G=	ENSP00000495041.1:n.*94+6234G=
ENST00000643042.1:c.918G=	ENSP00000496674.1:n.918G=
ENST00000643619.1:c.*880G=	ENSP00000494378.1:n.*880G=
ENST00000643752.1:c.*623G=	ENSP00000495000.1:n.*623G=
ENST00000644088.1:c.*618G=	ENSP00000494066.1:n.*618G=
ENST00000644591.1:c.*623G=	ENSP00000496664.1:n.*623G=
ENST00000644895.1:c.*99+6234G=	ENSP00000493872.1:n.*99+6234G=
ENST00000645345.1:c.*869G=	ENSP00000495859.1:n.*869G=
ENST00000647524.1:c.*880G=	ENSP00000495077.1:n.*880G=
ENST00000373189.5:c.1297G=	ENSP00000362285.5:p.Ala433=
ENST00000469204.1:n.794G=
NM_001174098.1:c.*526G=	NP_001167569.1:n.*526G=
NM_018344.5:c.1297G=	NP_060814.4:p.Ala433=
NR_033413.1:n.1271G=
NR_033414.1:n.1044G=
XM_006717910.2:c.1063G=	XP_006717973.1:p.Ala355=
NM_001363518.1:c.1063G=	NP_001350447.1:p.Ala355=
XM_017016377.2:c.859G=	XP_016871866.1:p.Ala287=
XM_017016378.2:c.679G=	XP_016871867.1:p.Ala227=
NM_018344.6:c.1297G= MANE Select	NP_060814.4:p.Ala433=
NM_001174098.2:c.*526G=	NP_001167569.1:n.*526G=
NM_001363518.2:c.1063G=	NP_001350447.1:p.Ala355=
NR_033413.2:n.1265G=
NR_033414.2:n.1038G=