Canonical Allele Identifier: CA1918678477

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362382G= , CM000672.2:g.71362382G=	GRCh38
NC_000010.10:g.73122139G= , CM000672.1:g.73122139G=	GRCh37
NC_000010.9:g.72792145G=	NCBI36
NG_017066.1:g.48130G=
NG_017066.2:g.48124G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2678G=
ENST00000373189.6:c.1202G= MANE Select	ENSP00000362285.5:p.Arg401=
ENST00000479577.2:c.968G=	ENSP00000493995.1:p.Arg323=
ENST00000642198.1:c.*774G=	ENSP00000494827.1:n.*774G=
ENST00000642772.1:c.*94+6139G=	ENSP00000495041.1:n.*94+6139G=
ENST00000643042.1:c.823G=	ENSP00000496674.1:n.823G=
ENST00000643619.1:c.*785G=	ENSP00000494378.1:n.*785G=
ENST00000643752.1:c.*528G=	ENSP00000495000.1:n.*528G=
ENST00000644088.1:c.*523G=	ENSP00000494066.1:n.*523G=
ENST00000644591.1:c.*528G=	ENSP00000496664.1:n.*528G=
ENST00000644895.1:c.*99+6139G=	ENSP00000493872.1:n.*99+6139G=
ENST00000645345.1:c.*774G=	ENSP00000495859.1:n.*774G=
ENST00000647524.1:c.*785G=	ENSP00000495077.1:n.*785G=
ENST00000373189.5:c.1202G=	ENSP00000362285.5:p.Arg401=
ENST00000469204.1:n.699G=
NM_001174098.1:c.*431G=	NP_001167569.1:n.*431G=
NM_018344.5:c.1202G=	NP_060814.4:p.Arg401=
NR_033413.1:n.1176G=
NR_033414.1:n.949G=
XM_006717910.2:c.968G=	XP_006717973.1:p.Arg323=
NM_001363518.1:c.968G=	NP_001350447.1:p.Arg323=
XM_017016377.2:c.764G=	XP_016871866.1:p.Arg255=
XM_017016378.2:c.584G=	XP_016871867.1:p.Arg195=
NM_018344.6:c.1202G= MANE Select	NP_060814.4:p.Arg401=
NM_001174098.2:c.*431G=	NP_001167569.1:n.*431G=
NM_001363518.2:c.968G=	NP_001350447.1:p.Arg323=
NR_033413.2:n.1170G=
NR_033414.2:n.943G=