Canonical Allele Identifier: CA377113995

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121759G>C (hg19) ; chr10:g.71362002G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362002G>C , CM000672.2:g.71362002G>C	GRCh38
NC_000010.10:g.73121759G>C , CM000672.1:g.73121759G>C	GRCh37
NC_000010.9:g.72791765G>C	NCBI36
NG_017066.1:g.47750G>C
NG_017066.2:g.47744G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2298G>C
ENST00000373189.6:c.822G>C MANE Select	ENSP00000362285.5:p.Glu274Asp
ENST00000479577.2:c.588G>C	ENSP00000493995.1:p.Glu196Asp
ENST00000642198.1:c.*394G>C	ENSP00000494827.1:n.*394G>C
ENST00000642772.1:c.*94+5759G>C	ENSP00000495041.1:n.*94+5759G>C
ENST00000643042.1:c.443G>C	ENSP00000496674.1:n.443G>C
ENST00000643619.1:c.*405G>C	ENSP00000494378.1:n.*405G>C
ENST00000643752.1:c.*148G>C	ENSP00000495000.1:n.*148G>C
ENST00000644088.1:c.*143G>C	ENSP00000494066.1:n.*143G>C
ENST00000644591.1:c.*148G>C	ENSP00000496664.1:n.*148G>C
ENST00000644895.1:c.*99+5759G>C	ENSP00000493872.1:n.*99+5759G>C
ENST00000645345.1:c.*394G>C	ENSP00000495859.1:n.*394G>C
ENST00000647524.1:c.*405G>C	ENSP00000495077.1:n.*405G>C
ENST00000373189.5:c.822G>C	ENSP00000362285.5:p.Glu274Asp
ENST00000469204.1:n.319G>C
NM_001174098.1:c.*51G>C	NP_001167569.1:n.*51G>C
NM_018344.5:c.822G>C	NP_060814.4:p.Glu274Asp
NR_033413.1:n.796G>C
NR_033414.1:n.569G>C
XM_006717910.2:c.588G>C	XP_006717973.1:p.Glu196Asp
NM_001363518.1:c.588G>C	NP_001350447.1:p.Glu196Asp
XM_017016377.2:c.384G>C	XP_016871866.1:p.Glu128Asp
XM_017016378.2:c.204G>C	XP_016871867.1:p.Glu68Asp
NM_018344.6:c.822G>C MANE Select	NP_060814.4:p.Glu274Asp
NM_001174098.2:c.*51G>C	NP_001167569.1:n.*51G>C
NM_001363518.2:c.588G>C	NP_001350447.1:p.Glu196Asp
NR_033413.2:n.790G>C
NR_033414.2:n.563G>C