Canonical Allele Identifier: CA1918678569

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362586C= , CM000672.2:g.71362586C=	GRCh38
NC_000010.10:g.73122343C= , CM000672.1:g.73122343C=	GRCh37
NC_000010.9:g.72792349C=	NCBI36
NG_017066.1:g.48334C=
NG_017066.2:g.48328C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2882C=
ENST00000373189.6:c.1406C= MANE Select	ENSP00000362285.5:p.Thr469=
ENST00000479577.2:c.1172C=	ENSP00000493995.1:p.Thr391=
ENST00000642198.1:c.*978C=	ENSP00000494827.1:n.*978C=
ENST00000642772.1:c.*94+6343C=	ENSP00000495041.1:n.*94+6343C=
ENST00000643042.1:c.1027C=	ENSP00000496674.1:n.1027C=
ENST00000643619.1:c.*989C=	ENSP00000494378.1:n.*989C=
ENST00000643752.1:c.*732C=	ENSP00000495000.1:n.*732C=
ENST00000644088.1:c.*727C=	ENSP00000494066.1:n.*727C=
ENST00000644591.1:c.*732C=	ENSP00000496664.1:n.*732C=
ENST00000644895.1:c.*99+6343C=	ENSP00000493872.1:n.*99+6343C=
ENST00000645345.1:c.*978C=	ENSP00000495859.1:n.*978C=
ENST00000647524.1:c.*989C=	ENSP00000495077.1:n.*989C=
ENST00000373189.5:c.1406C=	ENSP00000362285.5:p.Thr469=
NM_001174098.1:c.*635C=	NP_001167569.1:n.*635C=
NM_018344.5:c.1406C=	NP_060814.4:p.Thr469=
NR_033413.1:n.1380C=
NR_033414.1:n.1153C=
XM_006717910.2:c.1172C=	XP_006717973.1:p.Thr391=
NM_001363518.1:c.1172C=	NP_001350447.1:p.Thr391=
XM_017016377.2:c.968C=	XP_016871866.1:p.Thr323=
XM_017016378.2:c.788C=	XP_016871867.1:p.Thr263=
NM_018344.6:c.1406C= MANE Select	NP_060814.4:p.Thr469=
NM_001174098.2:c.*635C=	NP_001167569.1:n.*635C=
NM_001363518.2:c.1172C=	NP_001350447.1:p.Thr391=
NR_033413.2:n.1374C=
NR_033414.2:n.1147C=