Canonical Allele Identifier: CA1918678629

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362707T= , CM000672.2:g.71362707T=	GRCh38
NC_000010.10:g.73122464T= , CM000672.1:g.73122464T=	GRCh37
NC_000010.9:g.72792470T=	NCBI36
NG_017066.1:g.48455T=
NG_017066.2:g.48449T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3003T=
ENST00000373189.6:c.*99T= MANE Select	ENSP00000362285.5:n.*99T=
ENST00000479577.2:c.*99T=	ENSP00000493995.1:n.*99T=
ENST00000642198.1:c.*1099T=	ENSP00000494827.1:n.*1099T=
ENST00000642772.1:c.*94+6464T=	ENSP00000495041.1:n.*94+6464T=
ENST00000643042.1:c.1148T=	ENSP00000496674.1:n.1148T=
ENST00000643619.1:c.*1110T=	ENSP00000494378.1:n.*1110T=
ENST00000643752.1:c.*853T=	ENSP00000495000.1:n.*853T=
ENST00000644088.1:c.*848T=	ENSP00000494066.1:n.*848T=
ENST00000644591.1:c.*853T=	ENSP00000496664.1:n.*853T=
ENST00000644895.1:c.*99+6464T=	ENSP00000493872.1:n.*99+6464T=
ENST00000645345.1:c.*1099T=	ENSP00000495859.1:n.*1099T=
ENST00000647524.1:c.*1110T=	ENSP00000495077.1:n.*1110T=
ENST00000373189.5:c.*99T=	ENSP00000362285.5:n.*99T=
NM_001174098.1:c.*756T=	NP_001167569.1:n.*756T=
NM_018344.5:c.*99T=	NP_060814.4:n.*99T=
NR_033413.1:n.1501T=
NR_033414.1:n.1274T=
XM_006717910.2:c.*99T=	XP_006717973.1:n.*99T=
NM_001363518.1:c.*99T=	NP_001350447.1:n.*99T=
XM_017016377.2:c.*99T=	XP_016871866.1:n.*99T=
XM_017016378.2:c.*99T=	XP_016871867.1:n.*99T=
NM_018344.6:c.*99T= MANE Select	NP_060814.4:n.*99T=
NM_001174098.2:c.*756T=	NP_001167569.1:n.*756T=
NM_001363518.2:c.*99T=	NP_001350447.1:n.*99T=
NR_033413.2:n.1495T=
NR_033414.2:n.1268T=