Canonical Allele Identifier: CA1918678398

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362194C= , CM000672.2:g.71362194C=	GRCh38
NC_000010.10:g.73121951C= , CM000672.1:g.73121951C=	GRCh37
NC_000010.9:g.72791957C=	NCBI36
NG_017066.1:g.47942C=
NG_017066.2:g.47936C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2490C=
ENST00000373189.6:c.1014C= MANE Select	ENSP00000362285.5:p.Gly338=
ENST00000479577.2:c.780C=	ENSP00000493995.1:p.Gly260=
ENST00000642198.1:c.*586C=	ENSP00000494827.1:n.*586C=
ENST00000642772.1:c.*94+5951C=	ENSP00000495041.1:n.*94+5951C=
ENST00000643042.1:c.635C=	ENSP00000496674.1:n.635C=
ENST00000643619.1:c.*597C=	ENSP00000494378.1:n.*597C=
ENST00000643752.1:c.*340C=	ENSP00000495000.1:n.*340C=
ENST00000644088.1:c.*335C=	ENSP00000494066.1:n.*335C=
ENST00000644591.1:c.*340C=	ENSP00000496664.1:n.*340C=
ENST00000644895.1:c.*99+5951C=	ENSP00000493872.1:n.*99+5951C=
ENST00000645345.1:c.*586C=	ENSP00000495859.1:n.*586C=
ENST00000647524.1:c.*597C=	ENSP00000495077.1:n.*597C=
ENST00000373189.5:c.1014C=	ENSP00000362285.5:p.Gly338=
ENST00000469204.1:n.511C=
NM_001174098.1:c.*243C=	NP_001167569.1:n.*243C=
NM_018344.5:c.1014C=	NP_060814.4:p.Gly338=
NR_033413.1:n.988C=
NR_033414.1:n.761C=
XM_006717910.2:c.780C=	XP_006717973.1:p.Gly260=
NM_001363518.1:c.780C=	NP_001350447.1:p.Gly260=
XM_017016377.2:c.576C=	XP_016871866.1:p.Gly192=
XM_017016378.2:c.396C=	XP_016871867.1:p.Gly132=
NM_018344.6:c.1014C= MANE Select	NP_060814.4:p.Gly338=
NM_001174098.2:c.*243C=	NP_001167569.1:n.*243C=
NM_001363518.2:c.780C=	NP_001350447.1:p.Gly260=
NR_033413.2:n.982C=
NR_033414.2:n.755C=