Canonical Allele Identifier: CA1918678657

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362765A= , CM000672.2:g.71362765A=	GRCh38
NC_000010.10:g.73122522A= , CM000672.1:g.73122522A=	GRCh37
NC_000010.9:g.72792528A=	NCBI36
NG_017066.1:g.48513A=
NG_017066.2:g.48507A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3061A=
ENST00000373189.6:c.*157A= MANE Select	ENSP00000362285.5:n.*157A=
ENST00000479577.2:c.*157A=	ENSP00000493995.1:n.*157A=
ENST00000642198.1:c.*1157A=	ENSP00000494827.1:n.*1157A=
ENST00000642772.1:c.*94+6522A=	ENSP00000495041.1:n.*94+6522A=
ENST00000643042.1:c.1206A=	ENSP00000496674.1:n.1206A=
ENST00000643619.1:c.*1168A=	ENSP00000494378.1:n.*1168A=
ENST00000643752.1:c.*911A=	ENSP00000495000.1:n.*911A=
ENST00000644088.1:c.*906A=	ENSP00000494066.1:n.*906A=
ENST00000644591.1:c.*911A=	ENSP00000496664.1:n.*911A=
ENST00000644895.1:c.*99+6522A=	ENSP00000493872.1:n.*99+6522A=
ENST00000645345.1:c.*1157A=	ENSP00000495859.1:n.*1157A=
ENST00000647524.1:c.*1168A=	ENSP00000495077.1:n.*1168A=
ENST00000373189.5:c.*157A=	ENSP00000362285.5:n.*157A=
NM_001174098.1:c.*814A=	NP_001167569.1:n.*814A=
NM_018344.5:c.*157A=	NP_060814.4:n.*157A=
NR_033413.1:n.1559A=
NR_033414.1:n.1332A=
XM_006717910.2:c.*157A=	XP_006717973.1:n.*157A=
NM_001363518.1:c.*157A=	NP_001350447.1:n.*157A=
XM_017016377.2:c.*157A=	XP_016871866.1:n.*157A=
XM_017016378.2:c.*157A=	XP_016871867.1:n.*157A=
NM_018344.6:c.*157A= MANE Select	NP_060814.4:n.*157A=
NM_001174098.2:c.*814A=	NP_001167569.1:n.*814A=
NM_001363518.2:c.*157A=	NP_001350447.1:n.*157A=
NR_033413.2:n.1553A=
NR_033414.2:n.1326A=