Canonical Allele Identifier: CA1918678319

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362046G= , CM000672.2:g.71362046G=	GRCh38
NC_000010.10:g.73121803G= , CM000672.1:g.73121803G=	GRCh37
NC_000010.9:g.72791809G=	NCBI36
NG_017066.1:g.47794G=
NG_017066.2:g.47788G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2342G=
ENST00000373189.6:c.866G= MANE Select	ENSP00000362285.5:p.Arg289=
ENST00000479577.2:c.632G=	ENSP00000493995.1:p.Arg211=
ENST00000642198.1:c.*438G=	ENSP00000494827.1:n.*438G=
ENST00000642772.1:c.*94+5803G=	ENSP00000495041.1:n.*94+5803G=
ENST00000643042.1:c.487G=	ENSP00000496674.1:n.487G=
ENST00000643619.1:c.*449G=	ENSP00000494378.1:n.*449G=
ENST00000643752.1:c.*192G=	ENSP00000495000.1:n.*192G=
ENST00000644088.1:c.*187G=	ENSP00000494066.1:n.*187G=
ENST00000644591.1:c.*192G=	ENSP00000496664.1:n.*192G=
ENST00000644895.1:c.*99+5803G=	ENSP00000493872.1:n.*99+5803G=
ENST00000645345.1:c.*438G=	ENSP00000495859.1:n.*438G=
ENST00000647524.1:c.*449G=	ENSP00000495077.1:n.*449G=
ENST00000373189.5:c.866G=	ENSP00000362285.5:p.Arg289=
ENST00000469204.1:n.363G=
NM_001174098.1:c.*95G=	NP_001167569.1:n.*95G=
NM_018344.5:c.866G=	NP_060814.4:p.Arg289=
NR_033413.1:n.840G=
NR_033414.1:n.613G=
XM_006717910.2:c.632G=	XP_006717973.1:p.Arg211=
NM_001363518.1:c.632G=	NP_001350447.1:p.Arg211=
XM_017016377.2:c.428G=	XP_016871866.1:p.Arg143=
XM_017016378.2:c.248G=	XP_016871867.1:p.Arg83=
NM_018344.6:c.866G= MANE Select	NP_060814.4:p.Arg289=
NM_001174098.2:c.*95G=	NP_001167569.1:n.*95G=
NM_001363518.2:c.632G=	NP_001350447.1:p.Arg211=
NR_033413.2:n.834G=
NR_033414.2:n.607G=