Canonical Allele Identifier: CA470281434
Gene: SLC29A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.73122047G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71362290G>A , CM000672.2:g.71362290G>A GRCh38
NC_000010.10:g.73122047G>A , CM000672.1:g.73122047G>A GRCh37
NC_000010.9:g.72792053G>A NCBI36
NG_017066.1:g.48038G>A
NG_017066.2:g.48032G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000697843.1:n.2586G>A
ENST00000373189.6:c.1110G>A MANE Select ENSP00000362285.5:p.Gln370=
ENST00000479577.2:c.876G>A ENSP00000493995.1:p.Gln292=
ENST00000642198.1:c.*682G>A ENSP00000494827.1:n.*682G>A
ENST00000642772.1:c.*94+6047G>A ENSP00000495041.1:n.*94+6047G>A
ENST00000643042.1:c.731G>A ENSP00000496674.1:n.731G>A
ENST00000643619.1:c.*693G>A ENSP00000494378.1:n.*693G>A
ENST00000643752.1:c.*436G>A ENSP00000495000.1:n.*436G>A
ENST00000644088.1:c.*431G>A ENSP00000494066.1:n.*431G>A
ENST00000644591.1:c.*436G>A ENSP00000496664.1:n.*436G>A
ENST00000644895.1:c.*99+6047G>A ENSP00000493872.1:n.*99+6047G>A
ENST00000645345.1:c.*682G>A ENSP00000495859.1:n.*682G>A
ENST00000647524.1:c.*693G>A ENSP00000495077.1:n.*693G>A
ENST00000373189.5:c.1110G>A ENSP00000362285.5:p.Gln370=
ENST00000469204.1:n.607G>A
NM_001174098.1:c.*339G>A NP_001167569.1:n.*339G>A
NM_018344.5:c.1110G>A NP_060814.4:p.Gln370=
NR_033413.1:n.1084G>A
NR_033414.1:n.857G>A
XM_006717910.2:c.876G>A XP_006717973.1:p.Gln292=
NM_001363518.1:c.876G>A NP_001350447.1:p.Gln292=
XM_017016377.2:c.672G>A XP_016871866.1:p.Gln224=
XM_017016378.2:c.492G>A XP_016871867.1:p.Gln164=
NM_018344.6:c.1110G>A MANE Select NP_060814.4:p.Gln370=
NM_001174098.2:c.*339G>A NP_001167569.1:n.*339G>A
NM_001363518.2:c.876G>A NP_001350447.1:p.Gln292=
NR_033413.2:n.1078G>A
NR_033414.2:n.851G>A