Canonical Allele Identifier: CA377117358

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362510-G-C
• MyVariant Identifiers: chr10:g.73122267G>C (hg19) ; chr10:g.71362510G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362510G>C , CM000672.2:g.71362510G>C	GRCh38
NC_000010.10:g.73122267G>C , CM000672.1:g.73122267G>C	GRCh37
NC_000010.9:g.72792273G>C	NCBI36
NG_017066.1:g.48258G>C
NG_017066.2:g.48252G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697843.1:n.2806G>C
ENST00000373189.6:c.1330G>C MANE Select	ENSP00000362285.5:p.Glu444Gln
ENST00000479577.2:c.1096G>C	ENSP00000493995.1:p.Glu366Gln
ENST00000642198.1:c.*902G>C	ENSP00000494827.1:n.*902G>C
ENST00000642772.1:c.*94+6267G>C	ENSP00000495041.1:n.*94+6267G>C
ENST00000643042.1:c.951G>C	ENSP00000496674.1:n.951G>C
ENST00000643619.1:c.*913G>C	ENSP00000494378.1:n.*913G>C
ENST00000643752.1:c.*656G>C	ENSP00000495000.1:n.*656G>C
ENST00000644088.1:c.*651G>C	ENSP00000494066.1:n.*651G>C
ENST00000644591.1:c.*656G>C	ENSP00000496664.1:n.*656G>C
ENST00000644895.1:c.*99+6267G>C	ENSP00000493872.1:n.*99+6267G>C
ENST00000645345.1:c.*902G>C	ENSP00000495859.1:n.*902G>C
ENST00000647524.1:c.*913G>C	ENSP00000495077.1:n.*913G>C
ENST00000373189.5:c.1330G>C	ENSP00000362285.5:p.Glu444Gln
ENST00000469204.1:n.827G>C
NM_001174098.1:c.*559G>C	NP_001167569.1:n.*559G>C
NM_018344.5:c.1330G>C	NP_060814.4:p.Glu444Gln
NR_033413.1:n.1304G>C
NR_033414.1:n.1077G>C
XM_006717910.2:c.1096G>C	XP_006717973.1:p.Glu366Gln
NM_001363518.1:c.1096G>C	NP_001350447.1:p.Glu366Gln
XM_017016377.2:c.892G>C	XP_016871866.1:p.Glu298Gln
XM_017016378.2:c.712G>C	XP_016871867.1:p.Glu238Gln
NM_018344.6:c.1330G>C MANE Select	NP_060814.4:p.Glu444Gln
NM_001174098.2:c.*559G>C	NP_001167569.1:n.*559G>C
NM_001363518.2:c.1096G>C	NP_001350447.1:p.Glu366Gln
NR_033413.2:n.1298G>C
NR_033414.2:n.1071G>C