Canonical Allele Identifier: CA1918678302

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362015G= , CM000672.2:g.71362015G=	GRCh38
NC_000010.10:g.73121772G= , CM000672.1:g.73121772G=	GRCh37
NC_000010.9:g.72791778G=	NCBI36
NG_017066.1:g.47763G=
NG_017066.2:g.47757G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2311G=
ENST00000373189.6:c.835G= MANE Select	ENSP00000362285.5:p.Asp279=
ENST00000479577.2:c.601G=	ENSP00000493995.1:p.Asp201=
ENST00000642198.1:c.*407G=	ENSP00000494827.1:n.*407G=
ENST00000642772.1:c.*94+5772G=	ENSP00000495041.1:n.*94+5772G=
ENST00000643042.1:c.456G=	ENSP00000496674.1:n.456G=
ENST00000643619.1:c.*418G=	ENSP00000494378.1:n.*418G=
ENST00000643752.1:c.*161G=	ENSP00000495000.1:n.*161G=
ENST00000644088.1:c.*156G=	ENSP00000494066.1:n.*156G=
ENST00000644591.1:c.*161G=	ENSP00000496664.1:n.*161G=
ENST00000644895.1:c.*99+5772G=	ENSP00000493872.1:n.*99+5772G=
ENST00000645345.1:c.*407G=	ENSP00000495859.1:n.*407G=
ENST00000647524.1:c.*418G=	ENSP00000495077.1:n.*418G=
ENST00000373189.5:c.835G=	ENSP00000362285.5:p.Asp279=
ENST00000469204.1:n.332G=
NM_001174098.1:c.*64G=	NP_001167569.1:n.*64G=
NM_018344.5:c.835G=	NP_060814.4:p.Asp279=
NR_033413.1:n.809G=
NR_033414.1:n.582G=
XM_006717910.2:c.601G=	XP_006717973.1:p.Asp201=
NM_001363518.1:c.601G=	NP_001350447.1:p.Asp201=
XM_017016377.2:c.397G=	XP_016871866.1:p.Asp133=
XM_017016378.2:c.217G=	XP_016871867.1:p.Asp73=
NM_018344.6:c.835G= MANE Select	NP_060814.4:p.Asp279=
NM_001174098.2:c.*64G=	NP_001167569.1:n.*64G=
NM_001363518.2:c.601G=	NP_001350447.1:p.Asp201=
NR_033413.2:n.803G=
NR_033414.2:n.576G=