Canonical Allele Identifier: CA1918670550

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71344236G= , CM000672.2:g.71344236G=	GRCh38
NC_000010.10:g.73103993G= , CM000672.1:g.73103993G=	GRCh37
NC_000010.9:g.72773999G=	NCBI36
NG_017066.1:g.29984G=
NG_017066.2:g.29978G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.774G=
ENST00000373189.6:c.328G= MANE Select	ENSP00000362285.5:p.Ala110=
ENST00000479577.2:c.94G=	ENSP00000493995.1:p.Ala32=
ENST00000642198.1:c.67-7326G=	ENSP00000494827.1:n.67-7326G=
ENST00000642772.1:c.301-11845G=	ENSP00000495041.1:n.301-11845G=
ENST00000643042.1:c.232-11845G=	ENSP00000496674.1:n.232-11845G=
ENST00000643619.1:c.94G=	ENSP00000494378.1:p.Ala32=
ENST00000643752.1:c.328G=	ENSP00000495000.1:p.Ala110=
ENST00000644088.1:c.301-11845G=	ENSP00000494066.1:n.301-11845G=
ENST00000644591.1:c.301-7326G=	ENSP00000496664.1:n.301-7326G=
ENST00000644895.1:c.301-7326G=	ENSP00000493872.1:n.301-7326G=
ENST00000645345.1:c.301-7326G=	ENSP00000495859.1:n.301-7326G=
ENST00000647524.1:c.328G=	ENSP00000495077.1:p.Ala110=
ENST00000373189.5:c.328G=	ENSP00000362285.5:p.Ala110=
NM_001174098.1:c.328G=	NP_001167569.1:p.Ala110=
NM_018344.5:c.328G=	NP_060814.4:p.Ala110=
NR_033413.1:n.358-7326G=
NR_033414.1:n.358-11845G=
XM_006717910.2:c.94G=	XP_006717973.1:p.Ala32=
XR_946051.1:n.626-2855C=
NM_001363518.1:c.94G=	NP_001350447.1:p.Ala32=
XM_017016377.2:c.-55-7326G=	XP_016871866.1:n.-55-7326G=
XM_017016378.2:c.-8-11845G=	XP_016871867.1:n.-8-11845G=
XR_001747496.1:n.1552-2855C=
XR_001747497.1:n.8C=
XR_946051.2:n.1552-2855C=
NM_018344.6:c.328G= MANE Select	NP_060814.4:p.Ala110=
NM_001174098.2:c.328G=	NP_001167569.1:p.Ala110=
NM_001363518.2:c.94G=	NP_001350447.1:p.Ala32=
NR_033413.2:n.352-7326G=
NR_033414.2:n.352-11845G=