Canonical Allele Identifier: CA5543149

Gene: SLC29A3

Linked Data

• ClinVar Variation Id: 1552201
• ClinVar RCV Id: RCV002184806
• dbSNP Id: rs762952345
• ExAC: 10:73122140 C / T
• gnomAD v2: 10-73122140-C-T
• gnomAD v3: 10-71362383-C-T
• gnomAD v4: 10-71362383-C-T
• MyVariant Identifiers: chr10:g.73122140C>T (hg19) ; chr10:g.71362383C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362383C>T , CM000672.2:g.71362383C>T	GRCh38
NC_000010.10:g.73122140C>T , CM000672.1:g.73122140C>T	GRCh37
NC_000010.9:g.72792146C>T	NCBI36
NG_017066.1:g.48131C>T
NG_017066.2:g.48125C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2679C>T
ENST00000373189.6:c.1203C>T MANE Select	ENSP00000362285.5:p.Arg401=
ENST00000479577.2:c.969C>T	ENSP00000493995.1:p.Arg323=
ENST00000642198.1:c.*775C>T	ENSP00000494827.1:n.*775C>T
ENST00000642772.1:c.*94+6140C>T	ENSP00000495041.1:n.*94+6140C>T
ENST00000643042.1:c.824C>T	ENSP00000496674.1:n.824C>T
ENST00000643619.1:c.*786C>T	ENSP00000494378.1:n.*786C>T
ENST00000643752.1:c.*529C>T	ENSP00000495000.1:n.*529C>T
ENST00000644088.1:c.*524C>T	ENSP00000494066.1:n.*524C>T
ENST00000644591.1:c.*529C>T	ENSP00000496664.1:n.*529C>T
ENST00000644895.1:c.*99+6140C>T	ENSP00000493872.1:n.*99+6140C>T
ENST00000645345.1:c.*775C>T	ENSP00000495859.1:n.*775C>T
ENST00000647524.1:c.*786C>T	ENSP00000495077.1:n.*786C>T
ENST00000373189.5:c.1203C>T	ENSP00000362285.5:p.Arg401=
ENST00000469204.1:n.700C>T
NM_001174098.1:c.*432C>T	NP_001167569.1:n.*432C>T
NM_018344.5:c.1203C>T	NP_060814.4:p.Arg401=
NR_033413.1:n.1177C>T
NR_033414.1:n.950C>T
XM_006717910.2:c.969C>T	XP_006717973.1:p.Arg323=
NM_001363518.1:c.969C>T	NP_001350447.1:p.Arg323=
XM_017016377.2:c.765C>T	XP_016871866.1:p.Arg255=
XM_017016378.2:c.585C>T	XP_016871867.1:p.Arg195=
NM_018344.6:c.1203C>T MANE Select	NP_060814.4:p.Arg401=
NM_001174098.2:c.*432C>T	NP_001167569.1:n.*432C>T
NM_001363518.2:c.969C>T	NP_001350447.1:p.Arg323=
NR_033413.2:n.1171C>T
NR_033414.2:n.944C>T