Canonical Allele Identifier: CA1918678313

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362036G= , CM000672.2:g.71362036G=	GRCh38
NC_000010.10:g.73121793G= , CM000672.1:g.73121793G=	GRCh37
NC_000010.9:g.72791799G=	NCBI36
NG_017066.1:g.47784G=
NG_017066.2:g.47778G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2332G=
ENST00000373189.6:c.856G= MANE Select	ENSP00000362285.5:p.Val286=
ENST00000479577.2:c.622G=	ENSP00000493995.1:p.Val208=
ENST00000642198.1:c.*428G=	ENSP00000494827.1:n.*428G=
ENST00000642772.1:c.*94+5793G=	ENSP00000495041.1:n.*94+5793G=
ENST00000643042.1:c.477G=	ENSP00000496674.1:n.477G=
ENST00000643619.1:c.*439G=	ENSP00000494378.1:n.*439G=
ENST00000643752.1:c.*182G=	ENSP00000495000.1:n.*182G=
ENST00000644088.1:c.*177G=	ENSP00000494066.1:n.*177G=
ENST00000644591.1:c.*182G=	ENSP00000496664.1:n.*182G=
ENST00000644895.1:c.*99+5793G=	ENSP00000493872.1:n.*99+5793G=
ENST00000645345.1:c.*428G=	ENSP00000495859.1:n.*428G=
ENST00000647524.1:c.*439G=	ENSP00000495077.1:n.*439G=
ENST00000373189.5:c.856G=	ENSP00000362285.5:p.Val286=
ENST00000469204.1:n.353G=
NM_001174098.1:c.*85G=	NP_001167569.1:n.*85G=
NM_018344.5:c.856G=	NP_060814.4:p.Val286=
NR_033413.1:n.830G=
NR_033414.1:n.603G=
XM_006717910.2:c.622G=	XP_006717973.1:p.Val208=
NM_001363518.1:c.622G=	NP_001350447.1:p.Val208=
XM_017016377.2:c.418G=	XP_016871866.1:p.Val140=
XM_017016378.2:c.238G=	XP_016871867.1:p.Val80=
NM_018344.6:c.856G= MANE Select	NP_060814.4:p.Val286=
NM_001174098.2:c.*85G=	NP_001167569.1:n.*85G=
NM_001363518.2:c.622G=	NP_001350447.1:p.Val208=
NR_033413.2:n.824G=
NR_033414.2:n.597G=