Canonical Allele Identifier: CA1918678375

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362156A= , CM000672.2:g.71362156A=	GRCh38
NC_000010.10:g.73121913A= , CM000672.1:g.73121913A=	GRCh37
NC_000010.9:g.72791919A=	NCBI36
NG_017066.1:g.47904A=
NG_017066.2:g.47898A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2452A=
ENST00000373189.6:c.976A= MANE Select	ENSP00000362285.5:p.Ile326=
ENST00000479577.2:c.742A=	ENSP00000493995.1:p.Ile248=
ENST00000642198.1:c.*548A=	ENSP00000494827.1:n.*548A=
ENST00000642772.1:c.*94+5913A=	ENSP00000495041.1:n.*94+5913A=
ENST00000643042.1:c.597A=	ENSP00000496674.1:n.597A=
ENST00000643619.1:c.*559A=	ENSP00000494378.1:n.*559A=
ENST00000643752.1:c.*302A=	ENSP00000495000.1:n.*302A=
ENST00000644088.1:c.*297A=	ENSP00000494066.1:n.*297A=
ENST00000644591.1:c.*302A=	ENSP00000496664.1:n.*302A=
ENST00000644895.1:c.*99+5913A=	ENSP00000493872.1:n.*99+5913A=
ENST00000645345.1:c.*548A=	ENSP00000495859.1:n.*548A=
ENST00000647524.1:c.*559A=	ENSP00000495077.1:n.*559A=
ENST00000373189.5:c.976A=	ENSP00000362285.5:p.Ile326=
ENST00000469204.1:n.473A=
NM_001174098.1:c.*205A=	NP_001167569.1:n.*205A=
NM_018344.5:c.976A=	NP_060814.4:p.Ile326=
NR_033413.1:n.950A=
NR_033414.1:n.723A=
XM_006717910.2:c.742A=	XP_006717973.1:p.Ile248=
NM_001363518.1:c.742A=	NP_001350447.1:p.Ile248=
XM_017016377.2:c.538A=	XP_016871866.1:p.Ile180=
XM_017016378.2:c.358A=	XP_016871867.1:p.Ile120=
NM_018344.6:c.976A= MANE Select	NP_060814.4:p.Ile326=
NM_001174098.2:c.*205A=	NP_001167569.1:n.*205A=
NM_001363518.2:c.742A=	NP_001350447.1:p.Ile248=
NR_033413.2:n.944A=
NR_033414.2:n.717A=