Canonical Allele Identifier: CA377116142

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122004A>T (hg19) ; chr10:g.71362247A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362247A>T , CM000672.2:g.71362247A>T	GRCh38
NC_000010.10:g.73122004A>T , CM000672.1:g.73122004A>T	GRCh37
NC_000010.9:g.72792010A>T	NCBI36
NG_017066.1:g.47995A>T
NG_017066.2:g.47989A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2543A>T
ENST00000373189.6:c.1067A>T MANE Select	ENSP00000362285.5:p.Asn356Ile
ENST00000479577.2:c.833A>T	ENSP00000493995.1:p.Asn278Ile
ENST00000642198.1:c.*639A>T	ENSP00000494827.1:n.*639A>T
ENST00000642772.1:c.*94+6004A>T	ENSP00000495041.1:n.*94+6004A>T
ENST00000643042.1:c.688A>T	ENSP00000496674.1:n.688A>T
ENST00000643619.1:c.*650A>T	ENSP00000494378.1:n.*650A>T
ENST00000643752.1:c.*393A>T	ENSP00000495000.1:n.*393A>T
ENST00000644088.1:c.*388A>T	ENSP00000494066.1:n.*388A>T
ENST00000644591.1:c.*393A>T	ENSP00000496664.1:n.*393A>T
ENST00000644895.1:c.*99+6004A>T	ENSP00000493872.1:n.*99+6004A>T
ENST00000645345.1:c.*639A>T	ENSP00000495859.1:n.*639A>T
ENST00000647524.1:c.*650A>T	ENSP00000495077.1:n.*650A>T
ENST00000373189.5:c.1067A>T	ENSP00000362285.5:p.Asn356Ile
ENST00000469204.1:n.564A>T
NM_001174098.1:c.*296A>T	NP_001167569.1:n.*296A>T
NM_018344.5:c.1067A>T	NP_060814.4:p.Asn356Ile
NR_033413.1:n.1041A>T
NR_033414.1:n.814A>T
XM_006717910.2:c.833A>T	XP_006717973.1:p.Asn278Ile
NM_001363518.1:c.833A>T	NP_001350447.1:p.Asn278Ile
XM_017016377.2:c.629A>T	XP_016871866.1:p.Asn210Ile
XM_017016378.2:c.449A>T	XP_016871867.1:p.Asn150Ile
NM_018344.6:c.1067A>T MANE Select	NP_060814.4:p.Asn356Ile
NM_001174098.2:c.*296A>T	NP_001167569.1:n.*296A>T
NM_001363518.2:c.833A>T	NP_001350447.1:p.Asn278Ile
NR_033413.2:n.1035A>T
NR_033414.2:n.808A>T