Canonical Allele Identifier: CA1918678480

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362386C= , CM000672.2:g.71362386C=	GRCh38
NC_000010.10:g.73122143C= , CM000672.1:g.73122143C=	GRCh37
NC_000010.9:g.72792149C=	NCBI36
NG_017066.1:g.48134C=
NG_017066.2:g.48128C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2682C=
ENST00000373189.6:c.1206C= MANE Select	ENSP00000362285.5:p.Val402=
ENST00000479577.2:c.972C=	ENSP00000493995.1:p.Val324=
ENST00000642198.1:c.*778C=	ENSP00000494827.1:n.*778C=
ENST00000642772.1:c.*94+6143C=	ENSP00000495041.1:n.*94+6143C=
ENST00000643042.1:c.827C=	ENSP00000496674.1:n.827C=
ENST00000643619.1:c.*789C=	ENSP00000494378.1:n.*789C=
ENST00000643752.1:c.*532C=	ENSP00000495000.1:n.*532C=
ENST00000644088.1:c.*527C=	ENSP00000494066.1:n.*527C=
ENST00000644591.1:c.*532C=	ENSP00000496664.1:n.*532C=
ENST00000644895.1:c.*99+6143C=	ENSP00000493872.1:n.*99+6143C=
ENST00000645345.1:c.*778C=	ENSP00000495859.1:n.*778C=
ENST00000647524.1:c.*789C=	ENSP00000495077.1:n.*789C=
ENST00000373189.5:c.1206C=	ENSP00000362285.5:p.Val402=
ENST00000469204.1:n.703C=
NM_001174098.1:c.*435C=	NP_001167569.1:n.*435C=
NM_018344.5:c.1206C=	NP_060814.4:p.Val402=
NR_033413.1:n.1180C=
NR_033414.1:n.953C=
XM_006717910.2:c.972C=	XP_006717973.1:p.Val324=
NM_001363518.1:c.972C=	NP_001350447.1:p.Val324=
XM_017016377.2:c.768C=	XP_016871866.1:p.Val256=
XM_017016378.2:c.588C=	XP_016871867.1:p.Val196=
NM_018344.6:c.1206C= MANE Select	NP_060814.4:p.Val402=
NM_001174098.2:c.*435C=	NP_001167569.1:n.*435C=
NM_001363518.2:c.972C=	NP_001350447.1:p.Val324=
NR_033413.2:n.1174C=
NR_033414.2:n.947C=