Canonical Allele Identifier: CA1918678284

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361970G= , CM000672.2:g.71361970G=	GRCh38
NC_000010.10:g.73121727G= , CM000672.1:g.73121727G=	GRCh37
NC_000010.9:g.72791733G=	NCBI36
NG_017066.1:g.47718G=
NG_017066.2:g.47712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2266G=
ENST00000373189.6:c.790G= MANE Select	ENSP00000362285.5:p.Val264=
ENST00000479577.2:c.556G=	ENSP00000493995.1:p.Val186=
ENST00000642198.1:c.*362G=	ENSP00000494827.1:n.*362G=
ENST00000642772.1:c.*94+5727G=	ENSP00000495041.1:n.*94+5727G=
ENST00000643042.1:c.411G=	ENSP00000496674.1:n.411G=
ENST00000643619.1:c.*373G=	ENSP00000494378.1:n.*373G=
ENST00000643752.1:c.*116G=	ENSP00000495000.1:n.*116G=
ENST00000644088.1:c.*111G=	ENSP00000494066.1:n.*111G=
ENST00000644591.1:c.*116G=	ENSP00000496664.1:n.*116G=
ENST00000644895.1:c.*99+5727G=	ENSP00000493872.1:n.*99+5727G=
ENST00000645345.1:c.*362G=	ENSP00000495859.1:n.*362G=
ENST00000647524.1:c.*373G=	ENSP00000495077.1:n.*373G=
ENST00000373189.5:c.790G=	ENSP00000362285.5:p.Val264=
ENST00000469204.1:n.287G=
NM_001174098.1:c.*19G=	NP_001167569.1:n.*19G=
NM_018344.5:c.790G=	NP_060814.4:p.Val264=
NR_033413.1:n.764G=
NR_033414.1:n.537G=
XM_006717910.2:c.556G=	XP_006717973.1:p.Val186=
NM_001363518.1:c.556G=	NP_001350447.1:p.Val186=
XM_017016377.2:c.352G=	XP_016871866.1:p.Val118=
XM_017016378.2:c.172G=	XP_016871867.1:p.Val58=
NM_018344.6:c.790G= MANE Select	NP_060814.4:p.Val264=
NM_001174098.2:c.*19G=	NP_001167569.1:n.*19G=
NM_001363518.2:c.556G=	NP_001350447.1:p.Val186=
NR_033413.2:n.758G=
NR_033414.2:n.531G=