Canonical Allele Identifier: CA377114769

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121854C>T (hg19) ; chr10:g.71362097C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362097C>T , CM000672.2:g.71362097C>T	GRCh38
NC_000010.10:g.73121854C>T , CM000672.1:g.73121854C>T	GRCh37
NC_000010.9:g.72791860C>T	NCBI36
NG_017066.1:g.47845C>T
NG_017066.2:g.47839C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2393C>T
ENST00000373189.6:c.917C>T MANE Select	ENSP00000362285.5:p.Ala306Val
ENST00000479577.2:c.683C>T	ENSP00000493995.1:p.Ala228Val
ENST00000642198.1:c.*489C>T	ENSP00000494827.1:n.*489C>T
ENST00000642772.1:c.*94+5854C>T	ENSP00000495041.1:n.*94+5854C>T
ENST00000643042.1:c.538C>T	ENSP00000496674.1:n.538C>T
ENST00000643619.1:c.*500C>T	ENSP00000494378.1:n.*500C>T
ENST00000643752.1:c.*243C>T	ENSP00000495000.1:n.*243C>T
ENST00000644088.1:c.*238C>T	ENSP00000494066.1:n.*238C>T
ENST00000644591.1:c.*243C>T	ENSP00000496664.1:n.*243C>T
ENST00000644895.1:c.*99+5854C>T	ENSP00000493872.1:n.*99+5854C>T
ENST00000645345.1:c.*489C>T	ENSP00000495859.1:n.*489C>T
ENST00000647524.1:c.*500C>T	ENSP00000495077.1:n.*500C>T
ENST00000373189.5:c.917C>T	ENSP00000362285.5:p.Ala306Val
ENST00000469204.1:n.414C>T
NM_001174098.1:c.*146C>T	NP_001167569.1:n.*146C>T
NM_018344.5:c.917C>T	NP_060814.4:p.Ala306Val
NR_033413.1:n.891C>T
NR_033414.1:n.664C>T
XM_006717910.2:c.683C>T	XP_006717973.1:p.Ala228Val
NM_001363518.1:c.683C>T	NP_001350447.1:p.Ala228Val
XM_017016377.2:c.479C>T	XP_016871866.1:p.Ala160Val
XM_017016378.2:c.299C>T	XP_016871867.1:p.Ala100Val
NM_018344.6:c.917C>T MANE Select	NP_060814.4:p.Ala306Val
NM_001174098.2:c.*146C>T	NP_001167569.1:n.*146C>T
NM_001363518.2:c.683C>T	NP_001350447.1:p.Ala228Val
NR_033413.2:n.885C>T
NR_033414.2:n.658C>T