Canonical Allele Identifier: CA1918678488

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362401G= , CM000672.2:g.71362401G=	GRCh38
NC_000010.10:g.73122158G= , CM000672.1:g.73122158G=	GRCh37
NC_000010.9:g.72792164G=	NCBI36
NG_017066.1:g.48149G=
NG_017066.2:g.48143G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2697G=
ENST00000373189.6:c.1221G= MANE Select	ENSP00000362285.5:p.Val407=
ENST00000479577.2:c.987G=	ENSP00000493995.1:p.Val329=
ENST00000642198.1:c.*793G=	ENSP00000494827.1:n.*793G=
ENST00000642772.1:c.*94+6158G=	ENSP00000495041.1:n.*94+6158G=
ENST00000643042.1:c.842G=	ENSP00000496674.1:n.842G=
ENST00000643619.1:c.*804G=	ENSP00000494378.1:n.*804G=
ENST00000643752.1:c.*547G=	ENSP00000495000.1:n.*547G=
ENST00000644088.1:c.*542G=	ENSP00000494066.1:n.*542G=
ENST00000644591.1:c.*547G=	ENSP00000496664.1:n.*547G=
ENST00000644895.1:c.*99+6158G=	ENSP00000493872.1:n.*99+6158G=
ENST00000645345.1:c.*793G=	ENSP00000495859.1:n.*793G=
ENST00000647524.1:c.*804G=	ENSP00000495077.1:n.*804G=
ENST00000373189.5:c.1221G=	ENSP00000362285.5:p.Val407=
ENST00000469204.1:n.718G=
NM_001174098.1:c.*450G=	NP_001167569.1:n.*450G=
NM_018344.5:c.1221G=	NP_060814.4:p.Val407=
NR_033413.1:n.1195G=
NR_033414.1:n.968G=
XM_006717910.2:c.987G=	XP_006717973.1:p.Val329=
NM_001363518.1:c.987G=	NP_001350447.1:p.Val329=
XM_017016377.2:c.783G=	XP_016871866.1:p.Val261=
XM_017016378.2:c.603G=	XP_016871867.1:p.Val201=
NM_018344.6:c.1221G= MANE Select	NP_060814.4:p.Val407=
NM_001174098.2:c.*450G=	NP_001167569.1:n.*450G=
NM_001363518.2:c.987G=	NP_001350447.1:p.Val329=
NR_033413.2:n.1189G=
NR_033414.2:n.962G=