Canonical Allele Identifier: CA377116762

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122060A>T (hg19) ; chr10:g.71362303A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362303A>T , CM000672.2:g.71362303A>T	GRCh38
NC_000010.10:g.73122060A>T , CM000672.1:g.73122060A>T	GRCh37
NC_000010.9:g.72792066A>T	NCBI36
NG_017066.1:g.48051A>T
NG_017066.2:g.48045A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697843.1:n.2599A>T
ENST00000373189.6:c.1123A>T MANE Select	ENSP00000362285.5:p.Asn375Tyr
ENST00000479577.2:c.889A>T	ENSP00000493995.1:p.Asn297Tyr
ENST00000642198.1:c.*695A>T	ENSP00000494827.1:n.*695A>T
ENST00000642772.1:c.*94+6060A>T	ENSP00000495041.1:n.*94+6060A>T
ENST00000643042.1:c.744A>T	ENSP00000496674.1:n.744A>T
ENST00000643619.1:c.*706A>T	ENSP00000494378.1:n.*706A>T
ENST00000643752.1:c.*449A>T	ENSP00000495000.1:n.*449A>T
ENST00000644088.1:c.*444A>T	ENSP00000494066.1:n.*444A>T
ENST00000644591.1:c.*449A>T	ENSP00000496664.1:n.*449A>T
ENST00000644895.1:c.*99+6060A>T	ENSP00000493872.1:n.*99+6060A>T
ENST00000645345.1:c.*695A>T	ENSP00000495859.1:n.*695A>T
ENST00000647524.1:c.*706A>T	ENSP00000495077.1:n.*706A>T
ENST00000373189.5:c.1123A>T	ENSP00000362285.5:p.Asn375Tyr
ENST00000469204.1:n.620A>T
NM_001174098.1:c.*352A>T	NP_001167569.1:n.*352A>T
NM_018344.5:c.1123A>T	NP_060814.4:p.Asn375Tyr
NR_033413.1:n.1097A>T
NR_033414.1:n.870A>T
XM_006717910.2:c.889A>T	XP_006717973.1:p.Asn297Tyr
NM_001363518.1:c.889A>T	NP_001350447.1:p.Asn297Tyr
XM_017016377.2:c.685A>T	XP_016871866.1:p.Asn229Tyr
XM_017016378.2:c.505A>T	XP_016871867.1:p.Asn169Tyr
NM_018344.6:c.1123A>T MANE Select	NP_060814.4:p.Asn375Tyr
NM_001174098.2:c.*352A>T	NP_001167569.1:n.*352A>T
NM_001363518.2:c.889A>T	NP_001350447.1:p.Asn297Tyr
NR_033413.2:n.1091A>T
NR_033414.2:n.864A>T