Canonical Allele Identifier: CA1918678279

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361963G= , CM000672.2:g.71361963G=	GRCh38
NC_000010.10:g.73121720G= , CM000672.1:g.73121720G=	GRCh37
NC_000010.9:g.72791726G=	NCBI36
NG_017066.1:g.47711G=
NG_017066.2:g.47705G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2259G=
ENST00000373189.6:c.783G= MANE Select	ENSP00000362285.5:p.Met261=
ENST00000479577.2:c.549G=	ENSP00000493995.1:p.Met183=
ENST00000642198.1:c.*355G=	ENSP00000494827.1:n.*355G=
ENST00000642772.1:c.*94+5720G=	ENSP00000495041.1:n.*94+5720G=
ENST00000643042.1:c.404G=	ENSP00000496674.1:n.404G=
ENST00000643619.1:c.*366G=	ENSP00000494378.1:n.*366G=
ENST00000643752.1:c.*109G=	ENSP00000495000.1:n.*109G=
ENST00000644088.1:c.*104G=	ENSP00000494066.1:n.*104G=
ENST00000644591.1:c.*109G=	ENSP00000496664.1:n.*109G=
ENST00000644895.1:c.*99+5720G=	ENSP00000493872.1:n.*99+5720G=
ENST00000645345.1:c.*355G=	ENSP00000495859.1:n.*355G=
ENST00000647524.1:c.*366G=	ENSP00000495077.1:n.*366G=
ENST00000373189.5:c.783G=	ENSP00000362285.5:p.Met261=
ENST00000469204.1:n.280G=
NM_001174098.1:c.*12G=	NP_001167569.1:n.*12G=
NM_018344.5:c.783G=	NP_060814.4:p.Met261=
NR_033413.1:n.757G=
NR_033414.1:n.530G=
XM_006717910.2:c.549G=	XP_006717973.1:p.Met183=
NM_001363518.1:c.549G=	NP_001350447.1:p.Met183=
XM_017016377.2:c.345G=	XP_016871866.1:p.Met115=
XM_017016378.2:c.165G=	XP_016871867.1:p.Met55=
NM_018344.6:c.783G= MANE Select	NP_060814.4:p.Met261=
NM_001174098.2:c.*12G=	NP_001167569.1:n.*12G=
NM_001363518.2:c.549G=	NP_001350447.1:p.Met183=
NR_033413.2:n.751G=
NR_033414.2:n.524G=