Canonical Allele Identifier: CA377116943

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362337-G-C
• MyVariant Identifiers: chr10:g.73122094G>C (hg19) ; chr10:g.71362337G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362337G>C , CM000672.2:g.71362337G>C	GRCh38
NC_000010.10:g.73122094G>C , CM000672.1:g.73122094G>C	GRCh37
NC_000010.9:g.72792100G>C	NCBI36
NG_017066.1:g.48085G>C
NG_017066.2:g.48079G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2633G>C
ENST00000373189.6:c.1157G>C MANE Select	ENSP00000362285.5:p.Arg386Pro
ENST00000479577.2:c.923G>C	ENSP00000493995.1:p.Arg308Pro
ENST00000642198.1:c.*729G>C	ENSP00000494827.1:n.*729G>C
ENST00000642772.1:c.*94+6094G>C	ENSP00000495041.1:n.*94+6094G>C
ENST00000643042.1:c.778G>C	ENSP00000496674.1:n.778G>C
ENST00000643619.1:c.*740G>C	ENSP00000494378.1:n.*740G>C
ENST00000643752.1:c.*483G>C	ENSP00000495000.1:n.*483G>C
ENST00000644088.1:c.*478G>C	ENSP00000494066.1:n.*478G>C
ENST00000644591.1:c.*483G>C	ENSP00000496664.1:n.*483G>C
ENST00000644895.1:c.*99+6094G>C	ENSP00000493872.1:n.*99+6094G>C
ENST00000645345.1:c.*729G>C	ENSP00000495859.1:n.*729G>C
ENST00000647524.1:c.*740G>C	ENSP00000495077.1:n.*740G>C
ENST00000373189.5:c.1157G>C	ENSP00000362285.5:p.Arg386Pro
ENST00000469204.1:n.654G>C
NM_001174098.1:c.*386G>C	NP_001167569.1:n.*386G>C
NM_018344.5:c.1157G>C	NP_060814.4:p.Arg386Pro
NR_033413.1:n.1131G>C
NR_033414.1:n.904G>C
XM_006717910.2:c.923G>C	XP_006717973.1:p.Arg308Pro
NM_001363518.1:c.923G>C	NP_001350447.1:p.Arg308Pro
XM_017016377.2:c.719G>C	XP_016871866.1:p.Arg240Pro
XM_017016378.2:c.539G>C	XP_016871867.1:p.Arg180Pro
NM_018344.6:c.1157G>C MANE Select	NP_060814.4:p.Arg386Pro
NM_001174098.2:c.*386G>C	NP_001167569.1:n.*386G>C
NM_001363518.2:c.923G>C	NP_001350447.1:p.Arg308Pro
NR_033413.2:n.1125G>C
NR_033414.2:n.898G>C