Canonical Allele Identifier: CA1918678504

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362424C= , CM000672.2:g.71362424C=	GRCh38
NC_000010.10:g.73122181C= , CM000672.1:g.73122181C=	GRCh37
NC_000010.9:g.72792187C=	NCBI36
NG_017066.1:g.48172C=
NG_017066.2:g.48166C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2720C=
ENST00000373189.6:c.1244C= MANE Select	ENSP00000362285.5:p.Pro415=
ENST00000479577.2:c.1010C=	ENSP00000493995.1:p.Pro337=
ENST00000642198.1:c.*816C=	ENSP00000494827.1:n.*816C=
ENST00000642772.1:c.*94+6181C=	ENSP00000495041.1:n.*94+6181C=
ENST00000643042.1:c.865C=	ENSP00000496674.1:n.865C=
ENST00000643619.1:c.*827C=	ENSP00000494378.1:n.*827C=
ENST00000643752.1:c.*570C=	ENSP00000495000.1:n.*570C=
ENST00000644088.1:c.*565C=	ENSP00000494066.1:n.*565C=
ENST00000644591.1:c.*570C=	ENSP00000496664.1:n.*570C=
ENST00000644895.1:c.*99+6181C=	ENSP00000493872.1:n.*99+6181C=
ENST00000645345.1:c.*816C=	ENSP00000495859.1:n.*816C=
ENST00000647524.1:c.*827C=	ENSP00000495077.1:n.*827C=
ENST00000373189.5:c.1244C=	ENSP00000362285.5:p.Pro415=
ENST00000469204.1:n.741C=
NM_001174098.1:c.*473C=	NP_001167569.1:n.*473C=
NM_018344.5:c.1244C=	NP_060814.4:p.Pro415=
NR_033413.1:n.1218C=
NR_033414.1:n.991C=
XM_006717910.2:c.1010C=	XP_006717973.1:p.Pro337=
NM_001363518.1:c.1010C=	NP_001350447.1:p.Pro337=
XM_017016377.2:c.806C=	XP_016871866.1:p.Pro269=
XM_017016378.2:c.626C=	XP_016871867.1:p.Pro209=
NM_018344.6:c.1244C= MANE Select	NP_060814.4:p.Pro415=
NM_001174098.2:c.*473C=	NP_001167569.1:n.*473C=
NM_001363518.2:c.1010C=	NP_001350447.1:p.Pro337=
NR_033413.2:n.1212C=
NR_033414.2:n.985C=