Canonical Allele Identifier: CA377116912

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122076C>T (hg19) ; chr10:g.71362319C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362319C>T , CM000672.2:g.71362319C>T	GRCh38
NC_000010.10:g.73122076C>T , CM000672.1:g.73122076C>T	GRCh37
NC_000010.9:g.72792082C>T	NCBI36
NG_017066.1:g.48067C>T
NG_017066.2:g.48061C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2615C>T
ENST00000373189.6:c.1139C>T MANE Select	ENSP00000362285.5:p.Pro380Leu
ENST00000479577.2:c.905C>T	ENSP00000493995.1:p.Pro302Leu
ENST00000642198.1:c.*711C>T	ENSP00000494827.1:n.*711C>T
ENST00000642772.1:c.*94+6076C>T	ENSP00000495041.1:n.*94+6076C>T
ENST00000643042.1:c.760C>T	ENSP00000496674.1:n.760C>T
ENST00000643619.1:c.*722C>T	ENSP00000494378.1:n.*722C>T
ENST00000643752.1:c.*465C>T	ENSP00000495000.1:n.*465C>T
ENST00000644088.1:c.*460C>T	ENSP00000494066.1:n.*460C>T
ENST00000644591.1:c.*465C>T	ENSP00000496664.1:n.*465C>T
ENST00000644895.1:c.*99+6076C>T	ENSP00000493872.1:n.*99+6076C>T
ENST00000645345.1:c.*711C>T	ENSP00000495859.1:n.*711C>T
ENST00000647524.1:c.*722C>T	ENSP00000495077.1:n.*722C>T
ENST00000373189.5:c.1139C>T	ENSP00000362285.5:p.Pro380Leu
ENST00000469204.1:n.636C>T
NM_001174098.1:c.*368C>T	NP_001167569.1:n.*368C>T
NM_018344.5:c.1139C>T	NP_060814.4:p.Pro380Leu
NR_033413.1:n.1113C>T
NR_033414.1:n.886C>T
XM_006717910.2:c.905C>T	XP_006717973.1:p.Pro302Leu
NM_001363518.1:c.905C>T	NP_001350447.1:p.Pro302Leu
XM_017016377.2:c.701C>T	XP_016871866.1:p.Pro234Leu
XM_017016378.2:c.521C>T	XP_016871867.1:p.Pro174Leu
NM_018344.6:c.1139C>T MANE Select	NP_060814.4:p.Pro380Leu
NM_001174098.2:c.*368C>T	NP_001167569.1:n.*368C>T
NM_001363518.2:c.905C>T	NP_001350447.1:p.Pro302Leu
NR_033413.2:n.1107C>T
NR_033414.2:n.880C>T