Canonical Allele Identifier: CA1918670492
Gene: SLC29A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71344128G= , CM000672.2:g.71344128G= GRCh38
NC_000010.10:g.73103885G= , CM000672.1:g.73103885G= GRCh37
NC_000010.9:g.72773891G= NCBI36
NG_017066.1:g.29876G=
NG_017066.2:g.29870G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697843.1:n.747-81G=
ENST00000373189.6:c.301-81G= MANE Select ENSP00000362285.5:n.301-81G=
ENST00000479577.2:c.67-81G= ENSP00000493995.1:n.67-81G=
ENST00000642198.1:c.67-7434G= ENSP00000494827.1:n.67-7434G=
ENST00000642772.1:c.301-11953G= ENSP00000495041.1:n.301-11953G=
ENST00000643042.1:c.232-11953G= ENSP00000496674.1:n.232-11953G=
ENST00000643619.1:c.67-81G= ENSP00000494378.1:n.67-81G=
ENST00000643752.1:c.301-81G= ENSP00000495000.1:n.301-81G=
ENST00000644088.1:c.301-11953G= ENSP00000494066.1:n.301-11953G=
ENST00000644591.1:c.301-7434G= ENSP00000496664.1:n.301-7434G=
ENST00000644895.1:c.301-7434G= ENSP00000493872.1:n.301-7434G=
ENST00000645345.1:c.301-7434G= ENSP00000495859.1:n.301-7434G=
ENST00000647524.1:c.301-81G= ENSP00000495077.1:n.301-81G=
ENST00000373189.5:c.301-81G= ENSP00000362285.5:n.301-81G=
NM_001174098.1:c.301-81G= NP_001167569.1:n.301-81G=
NM_018344.5:c.301-81G= NP_060814.4:n.301-81G=
NR_033413.1:n.358-7434G=
NR_033414.1:n.358-11953G=
XM_006717910.2:c.67-81G= XP_006717973.1:n.67-81G=
XR_946051.1:n.626-2747C=
NM_001363518.1:c.67-81G= NP_001350447.1:n.67-81G=
XM_017016377.2:c.-55-7434G= XP_016871866.1:n.-55-7434G=
XM_017016378.2:c.-8-11953G= XP_016871867.1:n.-8-11953G=
XR_001747496.1:n.1552-2747C=
XR_001747497.1:n.82+34C=
XR_946051.2:n.1552-2747C=
NM_018344.6:c.301-81G= MANE Select NP_060814.4:n.301-81G=
NM_001174098.2:c.301-81G= NP_001167569.1:n.301-81G=
NM_001363518.2:c.67-81G= NP_001350447.1:n.67-81G=
NR_033413.2:n.352-7434G=
NR_033414.2:n.352-11953G=