Canonical Allele Identifier: CA377113883

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71361985-G-A
• MyVariant Identifiers: chr10:g.73121742G>A (hg19) ; chr10:g.71361985G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361985G>A , CM000672.2:g.71361985G>A	GRCh38
NC_000010.10:g.73121742G>A , CM000672.1:g.73121742G>A	GRCh37
NC_000010.9:g.72791748G>A	NCBI36
NG_017066.1:g.47733G>A
NG_017066.2:g.47727G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2281G>A
ENST00000373189.6:c.805G>A MANE Select	ENSP00000362285.5:p.Val269Met
ENST00000479577.2:c.571G>A	ENSP00000493995.1:p.Val191Met
ENST00000642198.1:c.*377G>A	ENSP00000494827.1:n.*377G>A
ENST00000642772.1:c.*94+5742G>A	ENSP00000495041.1:n.*94+5742G>A
ENST00000643042.1:c.426G>A	ENSP00000496674.1:n.426G>A
ENST00000643619.1:c.*388G>A	ENSP00000494378.1:n.*388G>A
ENST00000643752.1:c.*131G>A	ENSP00000495000.1:n.*131G>A
ENST00000644088.1:c.*126G>A	ENSP00000494066.1:n.*126G>A
ENST00000644591.1:c.*131G>A	ENSP00000496664.1:n.*131G>A
ENST00000644895.1:c.*99+5742G>A	ENSP00000493872.1:n.*99+5742G>A
ENST00000645345.1:c.*377G>A	ENSP00000495859.1:n.*377G>A
ENST00000647524.1:c.*388G>A	ENSP00000495077.1:n.*388G>A
ENST00000373189.5:c.805G>A	ENSP00000362285.5:p.Val269Met
ENST00000469204.1:n.302G>A
NM_001174098.1:c.*34G>A	NP_001167569.1:n.*34G>A
NM_018344.5:c.805G>A	NP_060814.4:p.Val269Met
NR_033413.1:n.779G>A
NR_033414.1:n.552G>A
XM_006717910.2:c.571G>A	XP_006717973.1:p.Val191Met
NM_001363518.1:c.571G>A	NP_001350447.1:p.Val191Met
XM_017016377.2:c.367G>A	XP_016871866.1:p.Val123Met
XM_017016378.2:c.187G>A	XP_016871867.1:p.Val63Met
NM_018344.6:c.805G>A MANE Select	NP_060814.4:p.Val269Met
NM_001174098.2:c.*34G>A	NP_001167569.1:n.*34G>A
NM_001363518.2:c.571G>A	NP_001350447.1:p.Val191Met
NR_033413.2:n.773G>A
NR_033414.2:n.546G>A