Canonical Allele Identifier: CA1918678632

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362712G= , CM000672.2:g.71362712G=	GRCh38
NC_000010.10:g.73122469G= , CM000672.1:g.73122469G=	GRCh37
NC_000010.9:g.72792475G=	NCBI36
NG_017066.1:g.48460G=
NG_017066.2:g.48454G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3008G=
ENST00000373189.6:c.*104G= MANE Select	ENSP00000362285.5:n.*104G=
ENST00000479577.2:c.*104G=	ENSP00000493995.1:n.*104G=
ENST00000642198.1:c.*1104G=	ENSP00000494827.1:n.*1104G=
ENST00000642772.1:c.*94+6469G=	ENSP00000495041.1:n.*94+6469G=
ENST00000643042.1:c.1153G=	ENSP00000496674.1:n.1153G=
ENST00000643619.1:c.*1115G=	ENSP00000494378.1:n.*1115G=
ENST00000643752.1:c.*858G=	ENSP00000495000.1:n.*858G=
ENST00000644088.1:c.*853G=	ENSP00000494066.1:n.*853G=
ENST00000644591.1:c.*858G=	ENSP00000496664.1:n.*858G=
ENST00000644895.1:c.*99+6469G=	ENSP00000493872.1:n.*99+6469G=
ENST00000645345.1:c.*1104G=	ENSP00000495859.1:n.*1104G=
ENST00000647524.1:c.*1115G=	ENSP00000495077.1:n.*1115G=
ENST00000373189.5:c.*104G=	ENSP00000362285.5:n.*104G=
NM_001174098.1:c.*761G=	NP_001167569.1:n.*761G=
NM_018344.5:c.*104G=	NP_060814.4:n.*104G=
NR_033413.1:n.1506G=
NR_033414.1:n.1279G=
XM_006717910.2:c.*104G=	XP_006717973.1:n.*104G=
NM_001363518.1:c.*104G=	NP_001350447.1:n.*104G=
XM_017016377.2:c.*104G=	XP_016871866.1:n.*104G=
XM_017016378.2:c.*104G=	XP_016871867.1:n.*104G=
NM_018344.6:c.*104G= MANE Select	NP_060814.4:n.*104G=
NM_001174098.2:c.*761G=	NP_001167569.1:n.*761G=
NM_001363518.2:c.*104G=	NP_001350447.1:n.*104G=
NR_033413.2:n.1500G=
NR_033414.2:n.1273G=