Canonical Allele Identifier: CA1918678391

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362182C= , CM000672.2:g.71362182C=	GRCh38
NC_000010.10:g.73121939C= , CM000672.1:g.73121939C=	GRCh37
NC_000010.9:g.72791945C=	NCBI36
NG_017066.1:g.47930C=
NG_017066.2:g.47924C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2478C=
ENST00000373189.6:c.1002C= MANE Select	ENSP00000362285.5:p.Asn334=
ENST00000479577.2:c.768C=	ENSP00000493995.1:p.Asn256=
ENST00000642198.1:c.*574C=	ENSP00000494827.1:n.*574C=
ENST00000642772.1:c.*94+5939C=	ENSP00000495041.1:n.*94+5939C=
ENST00000643042.1:c.623C=	ENSP00000496674.1:n.623C=
ENST00000643619.1:c.*585C=	ENSP00000494378.1:n.*585C=
ENST00000643752.1:c.*328C=	ENSP00000495000.1:n.*328C=
ENST00000644088.1:c.*323C=	ENSP00000494066.1:n.*323C=
ENST00000644591.1:c.*328C=	ENSP00000496664.1:n.*328C=
ENST00000644895.1:c.*99+5939C=	ENSP00000493872.1:n.*99+5939C=
ENST00000645345.1:c.*574C=	ENSP00000495859.1:n.*574C=
ENST00000647524.1:c.*585C=	ENSP00000495077.1:n.*585C=
ENST00000373189.5:c.1002C=	ENSP00000362285.5:p.Asn334=
ENST00000469204.1:n.499C=
NM_001174098.1:c.*231C=	NP_001167569.1:n.*231C=
NM_018344.5:c.1002C=	NP_060814.4:p.Asn334=
NR_033413.1:n.976C=
NR_033414.1:n.749C=
XM_006717910.2:c.768C=	XP_006717973.1:p.Asn256=
NM_001363518.1:c.768C=	NP_001350447.1:p.Asn256=
XM_017016377.2:c.564C=	XP_016871866.1:p.Asn188=
XM_017016378.2:c.384C=	XP_016871867.1:p.Asn128=
NM_018344.6:c.1002C= MANE Select	NP_060814.4:p.Asn334=
NM_001174098.2:c.*231C=	NP_001167569.1:n.*231C=
NM_001363518.2:c.768C=	NP_001350447.1:p.Asn256=
NR_033413.2:n.970C=
NR_033414.2:n.743C=