Canonical Allele Identifier: CA377113969

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121756A>C (hg19) ; chr10:g.71361999A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361999A>C , CM000672.2:g.71361999A>C	GRCh38
NC_000010.10:g.73121756A>C , CM000672.1:g.73121756A>C	GRCh37
NC_000010.9:g.72791762A>C	NCBI36
NG_017066.1:g.47747A>C
NG_017066.2:g.47741A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2295A>C
ENST00000373189.6:c.819A>C MANE Select	ENSP00000362285.5:p.Glu273Asp
ENST00000479577.2:c.585A>C	ENSP00000493995.1:p.Glu195Asp
ENST00000642198.1:c.*391A>C	ENSP00000494827.1:n.*391A>C
ENST00000642772.1:c.*94+5756A>C	ENSP00000495041.1:n.*94+5756A>C
ENST00000643042.1:c.440A>C	ENSP00000496674.1:n.440A>C
ENST00000643619.1:c.*402A>C	ENSP00000494378.1:n.*402A>C
ENST00000643752.1:c.*145A>C	ENSP00000495000.1:n.*145A>C
ENST00000644088.1:c.*140A>C	ENSP00000494066.1:n.*140A>C
ENST00000644591.1:c.*145A>C	ENSP00000496664.1:n.*145A>C
ENST00000644895.1:c.*99+5756A>C	ENSP00000493872.1:n.*99+5756A>C
ENST00000645345.1:c.*391A>C	ENSP00000495859.1:n.*391A>C
ENST00000647524.1:c.*402A>C	ENSP00000495077.1:n.*402A>C
ENST00000373189.5:c.819A>C	ENSP00000362285.5:p.Glu273Asp
ENST00000469204.1:n.316A>C
NM_001174098.1:c.*48A>C	NP_001167569.1:n.*48A>C
NM_018344.5:c.819A>C	NP_060814.4:p.Glu273Asp
NR_033413.1:n.793A>C
NR_033414.1:n.566A>C
XM_006717910.2:c.585A>C	XP_006717973.1:p.Glu195Asp
NM_001363518.1:c.585A>C	NP_001350447.1:p.Glu195Asp
XM_017016377.2:c.381A>C	XP_016871866.1:p.Glu127Asp
XM_017016378.2:c.201A>C	XP_016871867.1:p.Glu67Asp
NM_018344.6:c.819A>C MANE Select	NP_060814.4:p.Glu273Asp
NM_001174098.2:c.*48A>C	NP_001167569.1:n.*48A>C
NM_001363518.2:c.585A>C	NP_001350447.1:p.Glu195Asp
NR_033413.2:n.787A>C
NR_033414.2:n.560A>C