Canonical Allele Identifier: CA377116305

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362257-C-A
• MyVariant Identifiers: chr10:g.73122014C>A (hg19) ; chr10:g.71362257C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362257C>A , CM000672.2:g.71362257C>A	GRCh38
NC_000010.10:g.73122014C>A , CM000672.1:g.73122014C>A	GRCh37
NC_000010.9:g.72792020C>A	NCBI36
NG_017066.1:g.48005C>A
NG_017066.2:g.47999C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2553C>A
ENST00000373189.6:c.1077C>A MANE Select	ENSP00000362285.5:p.Asp359Glu
ENST00000479577.2:c.843C>A	ENSP00000493995.1:p.Asp281Glu
ENST00000642198.1:c.*649C>A	ENSP00000494827.1:n.*649C>A
ENST00000642772.1:c.*94+6014C>A	ENSP00000495041.1:n.*94+6014C>A
ENST00000643042.1:c.698C>A	ENSP00000496674.1:n.698C>A
ENST00000643619.1:c.*660C>A	ENSP00000494378.1:n.*660C>A
ENST00000643752.1:c.*403C>A	ENSP00000495000.1:n.*403C>A
ENST00000644088.1:c.*398C>A	ENSP00000494066.1:n.*398C>A
ENST00000644591.1:c.*403C>A	ENSP00000496664.1:n.*403C>A
ENST00000644895.1:c.*99+6014C>A	ENSP00000493872.1:n.*99+6014C>A
ENST00000645345.1:c.*649C>A	ENSP00000495859.1:n.*649C>A
ENST00000647524.1:c.*660C>A	ENSP00000495077.1:n.*660C>A
ENST00000373189.5:c.1077C>A	ENSP00000362285.5:p.Asp359Glu
ENST00000469204.1:n.574C>A
NM_001174098.1:c.*306C>A	NP_001167569.1:n.*306C>A
NM_018344.5:c.1077C>A	NP_060814.4:p.Asp359Glu
NR_033413.1:n.1051C>A
NR_033414.1:n.824C>A
XM_006717910.2:c.843C>A	XP_006717973.1:p.Asp281Glu
NM_001363518.1:c.843C>A	NP_001350447.1:p.Asp281Glu
XM_017016377.2:c.639C>A	XP_016871866.1:p.Asp213Glu
XM_017016378.2:c.459C>A	XP_016871867.1:p.Asp153Glu
NM_018344.6:c.1077C>A MANE Select	NP_060814.4:p.Asp359Glu
NM_001174098.2:c.*306C>A	NP_001167569.1:n.*306C>A
NM_001363518.2:c.843C>A	NP_001350447.1:p.Asp281Glu
NR_033413.2:n.1045C>A
NR_033414.2:n.818C>A