Canonical Allele Identifier: CA1918670592

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71344313C= , CM000672.2:g.71344313C=	GRCh38
NC_000010.10:g.73104070C= , CM000672.1:g.73104070C=	GRCh37
NC_000010.9:g.72774076C=	NCBI36
NG_017066.1:g.30061C=
NG_017066.2:g.30055C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.829+22C=
ENST00000373189.6:c.383+22C= MANE Select	ENSP00000362285.5:n.383+22C=
ENST00000479577.2:c.149+22C=	ENSP00000493995.1:n.149+22C=
ENST00000642198.1:c.67-7249C=	ENSP00000494827.1:n.67-7249C=
ENST00000642772.1:c.301-11768C=	ENSP00000495041.1:n.301-11768C=
ENST00000643042.1:c.232-11768C=	ENSP00000496674.1:n.232-11768C=
ENST00000643619.1:c.149+22C=	ENSP00000494378.1:n.149+22C=
ENST00000643752.1:c.383+22C=	ENSP00000495000.1:n.383+22C=
ENST00000644088.1:c.301-11768C=	ENSP00000494066.1:n.301-11768C=
ENST00000644591.1:c.301-7249C=	ENSP00000496664.1:n.301-7249C=
ENST00000644895.1:c.301-7249C=	ENSP00000493872.1:n.301-7249C=
ENST00000645345.1:c.301-7249C=	ENSP00000495859.1:n.301-7249C=
ENST00000647524.1:c.383+22C=	ENSP00000495077.1:n.383+22C=
ENST00000373189.5:c.383+22C=	ENSP00000362285.5:n.383+22C=
NM_001174098.1:c.383+22C=	NP_001167569.1:n.383+22C=
NM_018344.5:c.383+22C=	NP_060814.4:n.383+22C=
NR_033413.1:n.358-7249C=
NR_033414.1:n.358-11768C=
XM_006717910.2:c.149+22C=	XP_006717973.1:n.149+22C=
XR_946051.1:n.626-2932G=
NM_001363518.1:c.149+22C=	NP_001350447.1:n.149+22C=
XM_017016377.2:c.-55-7249C=	XP_016871866.1:n.-55-7249C=
XM_017016378.2:c.-8-11768C=	XP_016871867.1:n.-8-11768C=
XR_001747496.1:n.1552-2932G=
XR_946051.2:n.1552-2932G=
NM_018344.6:c.383+22C= MANE Select	NP_060814.4:n.383+22C=
NM_001174098.2:c.383+22C=	NP_001167569.1:n.383+22C=
NM_001363518.2:c.149+22C=	NP_001350447.1:n.149+22C=
NR_033413.2:n.352-7249C=
NR_033414.2:n.352-11768C=