Canonical Allele Identifier: CA1918678320

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362051A= , CM000672.2:g.71362051A=	GRCh38
NC_000010.10:g.73121808A= , CM000672.1:g.73121808A=	GRCh37
NC_000010.9:g.72791814A=	NCBI36
NG_017066.1:g.47799A=
NG_017066.2:g.47793A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2347A=
ENST00000373189.6:c.871A= MANE Select	ENSP00000362285.5:p.Ile291=
ENST00000479577.2:c.637A=	ENSP00000493995.1:p.Ile213=
ENST00000642198.1:c.*443A=	ENSP00000494827.1:n.*443A=
ENST00000642772.1:c.*94+5808A=	ENSP00000495041.1:n.*94+5808A=
ENST00000643042.1:c.492A=	ENSP00000496674.1:n.492A=
ENST00000643619.1:c.*454A=	ENSP00000494378.1:n.*454A=
ENST00000643752.1:c.*197A=	ENSP00000495000.1:n.*197A=
ENST00000644088.1:c.*192A=	ENSP00000494066.1:n.*192A=
ENST00000644591.1:c.*197A=	ENSP00000496664.1:n.*197A=
ENST00000644895.1:c.*99+5808A=	ENSP00000493872.1:n.*99+5808A=
ENST00000645345.1:c.*443A=	ENSP00000495859.1:n.*443A=
ENST00000647524.1:c.*454A=	ENSP00000495077.1:n.*454A=
ENST00000373189.5:c.871A=	ENSP00000362285.5:p.Ile291=
ENST00000469204.1:n.368A=
NM_001174098.1:c.*100A=	NP_001167569.1:n.*100A=
NM_018344.5:c.871A=	NP_060814.4:p.Ile291=
NR_033413.1:n.845A=
NR_033414.1:n.618A=
XM_006717910.2:c.637A=	XP_006717973.1:p.Ile213=
NM_001363518.1:c.637A=	NP_001350447.1:p.Ile213=
XM_017016377.2:c.433A=	XP_016871866.1:p.Ile145=
XM_017016378.2:c.253A=	XP_016871867.1:p.Ile85=
NM_018344.6:c.871A= MANE Select	NP_060814.4:p.Ile291=
NM_001174098.2:c.*100A=	NP_001167569.1:n.*100A=
NM_001363518.2:c.637A=	NP_001350447.1:p.Ile213=
NR_033413.2:n.839A=
NR_033414.2:n.612A=