Canonical Allele Identifier: CA1918678303

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362017C= , CM000672.2:g.71362017C=	GRCh38
NC_000010.10:g.73121774C= , CM000672.1:g.73121774C=	GRCh37
NC_000010.9:g.72791780C=	NCBI36
NG_017066.1:g.47765C=
NG_017066.2:g.47759C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2313C=
ENST00000373189.6:c.837C= MANE Select	ENSP00000362285.5:p.Asp279=
ENST00000479577.2:c.603C=	ENSP00000493995.1:p.Asp201=
ENST00000642198.1:c.*409C=	ENSP00000494827.1:n.*409C=
ENST00000642772.1:c.*94+5774C=	ENSP00000495041.1:n.*94+5774C=
ENST00000643042.1:c.458C=	ENSP00000496674.1:n.458C=
ENST00000643619.1:c.*420C=	ENSP00000494378.1:n.*420C=
ENST00000643752.1:c.*163C=	ENSP00000495000.1:n.*163C=
ENST00000644088.1:c.*158C=	ENSP00000494066.1:n.*158C=
ENST00000644591.1:c.*163C=	ENSP00000496664.1:n.*163C=
ENST00000644895.1:c.*99+5774C=	ENSP00000493872.1:n.*99+5774C=
ENST00000645345.1:c.*409C=	ENSP00000495859.1:n.*409C=
ENST00000647524.1:c.*420C=	ENSP00000495077.1:n.*420C=
ENST00000373189.5:c.837C=	ENSP00000362285.5:p.Asp279=
ENST00000469204.1:n.334C=
NM_001174098.1:c.*66C=	NP_001167569.1:n.*66C=
NM_018344.5:c.837C=	NP_060814.4:p.Asp279=
NR_033413.1:n.811C=
NR_033414.1:n.584C=
XM_006717910.2:c.603C=	XP_006717973.1:p.Asp201=
NM_001363518.1:c.603C=	NP_001350447.1:p.Asp201=
XM_017016377.2:c.399C=	XP_016871866.1:p.Asp133=
XM_017016378.2:c.219C=	XP_016871867.1:p.Asp73=
NM_018344.6:c.837C= MANE Select	NP_060814.4:p.Asp279=
NM_001174098.2:c.*66C=	NP_001167569.1:n.*66C=
NM_001363518.2:c.603C=	NP_001350447.1:p.Asp201=
NR_033413.2:n.805C=
NR_033414.2:n.578C=