Canonical Allele Identifier: CA470281540

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362323-G-T
• MyVariant Identifiers: chr10:g.73122080G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362323G>T , CM000672.2:g.71362323G>T	GRCh38
NC_000010.10:g.73122080G>T , CM000672.1:g.73122080G>T	GRCh37
NC_000010.9:g.72792086G>T	NCBI36
NG_017066.1:g.48071G>T
NG_017066.2:g.48065G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2619G>T
ENST00000373189.6:c.1143G>T MANE Select	ENSP00000362285.5:p.Gly381=
ENST00000479577.2:c.909G>T	ENSP00000493995.1:p.Gly303=
ENST00000642198.1:c.*715G>T	ENSP00000494827.1:n.*715G>T
ENST00000642772.1:c.*94+6080G>T	ENSP00000495041.1:n.*94+6080G>T
ENST00000643042.1:c.764G>T	ENSP00000496674.1:n.764G>T
ENST00000643619.1:c.*726G>T	ENSP00000494378.1:n.*726G>T
ENST00000643752.1:c.*469G>T	ENSP00000495000.1:n.*469G>T
ENST00000644088.1:c.*464G>T	ENSP00000494066.1:n.*464G>T
ENST00000644591.1:c.*469G>T	ENSP00000496664.1:n.*469G>T
ENST00000644895.1:c.*99+6080G>T	ENSP00000493872.1:n.*99+6080G>T
ENST00000645345.1:c.*715G>T	ENSP00000495859.1:n.*715G>T
ENST00000647524.1:c.*726G>T	ENSP00000495077.1:n.*726G>T
ENST00000373189.5:c.1143G>T	ENSP00000362285.5:p.Gly381=
ENST00000469204.1:n.640G>T
NM_001174098.1:c.*372G>T	NP_001167569.1:n.*372G>T
NM_018344.5:c.1143G>T	NP_060814.4:p.Gly381=
NR_033413.1:n.1117G>T
NR_033414.1:n.890G>T
XM_006717910.2:c.909G>T	XP_006717973.1:p.Gly303=
NM_001363518.1:c.909G>T	NP_001350447.1:p.Gly303=
XM_017016377.2:c.705G>T	XP_016871866.1:p.Gly235=
XM_017016378.2:c.525G>T	XP_016871867.1:p.Gly175=
NM_018344.6:c.1143G>T MANE Select	NP_060814.4:p.Gly381=
NM_001174098.2:c.*372G>T	NP_001167569.1:n.*372G>T
NM_001363518.2:c.909G>T	NP_001350447.1:p.Gly303=
NR_033413.2:n.1111G>T
NR_033414.2:n.884G>T