Canonical Allele Identifier: CA1918678601

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362648A= , CM000672.2:g.71362648A=	GRCh38
NC_000010.10:g.73122405A= , CM000672.1:g.73122405A=	GRCh37
NC_000010.9:g.72792411A=	NCBI36
NG_017066.1:g.48396A=
NG_017066.2:g.48390A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2944A=
ENST00000373189.6:c.*40A= MANE Select	ENSP00000362285.5:n.*40A=
ENST00000479577.2:c.*40A=	ENSP00000493995.1:n.*40A=
ENST00000642198.1:c.*1040A=	ENSP00000494827.1:n.*1040A=
ENST00000642772.1:c.*94+6405A=	ENSP00000495041.1:n.*94+6405A=
ENST00000643042.1:c.1089A=	ENSP00000496674.1:n.1089A=
ENST00000643619.1:c.*1051A=	ENSP00000494378.1:n.*1051A=
ENST00000643752.1:c.*794A=	ENSP00000495000.1:n.*794A=
ENST00000644088.1:c.*789A=	ENSP00000494066.1:n.*789A=
ENST00000644591.1:c.*794A=	ENSP00000496664.1:n.*794A=
ENST00000644895.1:c.*99+6405A=	ENSP00000493872.1:n.*99+6405A=
ENST00000645345.1:c.*1040A=	ENSP00000495859.1:n.*1040A=
ENST00000647524.1:c.*1051A=	ENSP00000495077.1:n.*1051A=
ENST00000373189.5:c.*40A=	ENSP00000362285.5:n.*40A=
NM_001174098.1:c.*697A=	NP_001167569.1:n.*697A=
NM_018344.5:c.*40A=	NP_060814.4:n.*40A=
NR_033413.1:n.1442A=
NR_033414.1:n.1215A=
XM_006717910.2:c.*40A=	XP_006717973.1:n.*40A=
NM_001363518.1:c.*40A=	NP_001350447.1:n.*40A=
XM_017016377.2:c.*40A=	XP_016871866.1:n.*40A=
XM_017016378.2:c.*40A=	XP_016871867.1:n.*40A=
NM_018344.6:c.*40A= MANE Select	NP_060814.4:n.*40A=
NM_001174098.2:c.*697A=	NP_001167569.1:n.*697A=
NM_001363518.2:c.*40A=	NP_001350447.1:n.*40A=
NR_033413.2:n.1436A=
NR_033414.2:n.1209A=