Canonical Allele Identifier: CA377116280

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362255-G-A
• MyVariant Identifiers: chr10:g.73122012G>A (hg19) ; chr10:g.71362255G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362255G>A , CM000672.2:g.71362255G>A	GRCh38
NC_000010.10:g.73122012G>A , CM000672.1:g.73122012G>A	GRCh37
NC_000010.9:g.72792018G>A	NCBI36
NG_017066.1:g.48003G>A
NG_017066.2:g.47997G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2551G>A
ENST00000373189.6:c.1075G>A MANE Select	ENSP00000362285.5:p.Asp359Asn
ENST00000479577.2:c.841G>A	ENSP00000493995.1:p.Asp281Asn
ENST00000642198.1:c.*647G>A	ENSP00000494827.1:n.*647G>A
ENST00000642772.1:c.*94+6012G>A	ENSP00000495041.1:n.*94+6012G>A
ENST00000643042.1:c.696G>A	ENSP00000496674.1:n.696G>A
ENST00000643619.1:c.*658G>A	ENSP00000494378.1:n.*658G>A
ENST00000643752.1:c.*401G>A	ENSP00000495000.1:n.*401G>A
ENST00000644088.1:c.*396G>A	ENSP00000494066.1:n.*396G>A
ENST00000644591.1:c.*401G>A	ENSP00000496664.1:n.*401G>A
ENST00000644895.1:c.*99+6012G>A	ENSP00000493872.1:n.*99+6012G>A
ENST00000645345.1:c.*647G>A	ENSP00000495859.1:n.*647G>A
ENST00000647524.1:c.*658G>A	ENSP00000495077.1:n.*658G>A
ENST00000373189.5:c.1075G>A	ENSP00000362285.5:p.Asp359Asn
ENST00000469204.1:n.572G>A
NM_001174098.1:c.*304G>A	NP_001167569.1:n.*304G>A
NM_018344.5:c.1075G>A	NP_060814.4:p.Asp359Asn
NR_033413.1:n.1049G>A
NR_033414.1:n.822G>A
XM_006717910.2:c.841G>A	XP_006717973.1:p.Asp281Asn
NM_001363518.1:c.841G>A	NP_001350447.1:p.Asp281Asn
XM_017016377.2:c.637G>A	XP_016871866.1:p.Asp213Asn
XM_017016378.2:c.457G>A	XP_016871867.1:p.Asp153Asn
NM_018344.6:c.1075G>A MANE Select	NP_060814.4:p.Asp359Asn
NM_001174098.2:c.*304G>A	NP_001167569.1:n.*304G>A
NM_001363518.2:c.841G>A	NP_001350447.1:p.Asp281Asn
NR_033413.2:n.1043G>A
NR_033414.2:n.816G>A