Canonical Allele Identifier: CA377114103

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121773A>C (hg19) ; chr10:g.71362016A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362016A>C , CM000672.2:g.71362016A>C	GRCh38
NC_000010.10:g.73121773A>C , CM000672.1:g.73121773A>C	GRCh37
NC_000010.9:g.72791779A>C	NCBI36
NG_017066.1:g.47764A>C
NG_017066.2:g.47758A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2312A>C
ENST00000373189.6:c.836A>C MANE Select	ENSP00000362285.5:p.Asp279Ala
ENST00000479577.2:c.602A>C	ENSP00000493995.1:p.Asp201Ala
ENST00000642198.1:c.*408A>C	ENSP00000494827.1:n.*408A>C
ENST00000642772.1:c.*94+5773A>C	ENSP00000495041.1:n.*94+5773A>C
ENST00000643042.1:c.457A>C	ENSP00000496674.1:n.457A>C
ENST00000643619.1:c.*419A>C	ENSP00000494378.1:n.*419A>C
ENST00000643752.1:c.*162A>C	ENSP00000495000.1:n.*162A>C
ENST00000644088.1:c.*157A>C	ENSP00000494066.1:n.*157A>C
ENST00000644591.1:c.*162A>C	ENSP00000496664.1:n.*162A>C
ENST00000644895.1:c.*99+5773A>C	ENSP00000493872.1:n.*99+5773A>C
ENST00000645345.1:c.*408A>C	ENSP00000495859.1:n.*408A>C
ENST00000647524.1:c.*419A>C	ENSP00000495077.1:n.*419A>C
ENST00000373189.5:c.836A>C	ENSP00000362285.5:p.Asp279Ala
ENST00000469204.1:n.333A>C
NM_001174098.1:c.*65A>C	NP_001167569.1:n.*65A>C
NM_018344.5:c.836A>C	NP_060814.4:p.Asp279Ala
NR_033413.1:n.810A>C
NR_033414.1:n.583A>C
XM_006717910.2:c.602A>C	XP_006717973.1:p.Asp201Ala
NM_001363518.1:c.602A>C	NP_001350447.1:p.Asp201Ala
XM_017016377.2:c.398A>C	XP_016871866.1:p.Asp133Ala
XM_017016378.2:c.218A>C	XP_016871867.1:p.Asp73Ala
NM_018344.6:c.836A>C MANE Select	NP_060814.4:p.Asp279Ala
NM_001174098.2:c.*65A>C	NP_001167569.1:n.*65A>C
NM_001363518.2:c.602A>C	NP_001350447.1:p.Asp201Ala
NR_033413.2:n.804A>C
NR_033414.2:n.577A>C