Canonical Allele Identifier: CA377114294

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121800C>T (hg19) ; chr10:g.71362043C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362043C>T , CM000672.2:g.71362043C>T	GRCh38
NC_000010.10:g.73121800C>T , CM000672.1:g.73121800C>T	GRCh37
NC_000010.9:g.72791806C>T	NCBI36
NG_017066.1:g.47791C>T
NG_017066.2:g.47785C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2339C>T
ENST00000373189.6:c.863C>T MANE Select	ENSP00000362285.5:p.Ser288Phe
ENST00000479577.2:c.629C>T	ENSP00000493995.1:p.Ser210Phe
ENST00000642198.1:c.*435C>T	ENSP00000494827.1:n.*435C>T
ENST00000642772.1:c.*94+5800C>T	ENSP00000495041.1:n.*94+5800C>T
ENST00000643042.1:c.484C>T	ENSP00000496674.1:n.484C>T
ENST00000643619.1:c.*446C>T	ENSP00000494378.1:n.*446C>T
ENST00000643752.1:c.*189C>T	ENSP00000495000.1:n.*189C>T
ENST00000644088.1:c.*184C>T	ENSP00000494066.1:n.*184C>T
ENST00000644591.1:c.*189C>T	ENSP00000496664.1:n.*189C>T
ENST00000644895.1:c.*99+5800C>T	ENSP00000493872.1:n.*99+5800C>T
ENST00000645345.1:c.*435C>T	ENSP00000495859.1:n.*435C>T
ENST00000647524.1:c.*446C>T	ENSP00000495077.1:n.*446C>T
ENST00000373189.5:c.863C>T	ENSP00000362285.5:p.Ser288Phe
ENST00000469204.1:n.360C>T
NM_001174098.1:c.*92C>T	NP_001167569.1:n.*92C>T
NM_018344.5:c.863C>T	NP_060814.4:p.Ser288Phe
NR_033413.1:n.837C>T
NR_033414.1:n.610C>T
XM_006717910.2:c.629C>T	XP_006717973.1:p.Ser210Phe
NM_001363518.1:c.629C>T	NP_001350447.1:p.Ser210Phe
XM_017016377.2:c.425C>T	XP_016871866.1:p.Ser142Phe
XM_017016378.2:c.245C>T	XP_016871867.1:p.Ser82Phe
NM_018344.6:c.863C>T MANE Select	NP_060814.4:p.Ser288Phe
NM_001174098.2:c.*92C>T	NP_001167569.1:n.*92C>T
NM_001363518.2:c.629C>T	NP_001350447.1:p.Ser210Phe
NR_033413.2:n.831C>T
NR_033414.2:n.604C>T