Canonical Allele Identifier: CA1918678591

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362624G= , CM000672.2:g.71362624G=	GRCh38
NC_000010.10:g.73122381G= , CM000672.1:g.73122381G=	GRCh37
NC_000010.9:g.72792387G=	NCBI36
NG_017066.1:g.48372G=
NG_017066.2:g.48366G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2920G=
ENST00000373189.6:c.*16G= MANE Select	ENSP00000362285.5:n.*16G=
ENST00000479577.2:c.*16G=	ENSP00000493995.1:n.*16G=
ENST00000642198.1:c.*1016G=	ENSP00000494827.1:n.*1016G=
ENST00000642772.1:c.*94+6381G=	ENSP00000495041.1:n.*94+6381G=
ENST00000643042.1:c.1065G=	ENSP00000496674.1:n.1065G=
ENST00000643619.1:c.*1027G=	ENSP00000494378.1:n.*1027G=
ENST00000643752.1:c.*770G=	ENSP00000495000.1:n.*770G=
ENST00000644088.1:c.*765G=	ENSP00000494066.1:n.*765G=
ENST00000644591.1:c.*770G=	ENSP00000496664.1:n.*770G=
ENST00000644895.1:c.*99+6381G=	ENSP00000493872.1:n.*99+6381G=
ENST00000645345.1:c.*1016G=	ENSP00000495859.1:n.*1016G=
ENST00000647524.1:c.*1027G=	ENSP00000495077.1:n.*1027G=
ENST00000373189.5:c.*16G=	ENSP00000362285.5:n.*16G=
NM_001174098.1:c.*673G=	NP_001167569.1:n.*673G=
NM_018344.5:c.*16G=	NP_060814.4:n.*16G=
NR_033413.1:n.1418G=
NR_033414.1:n.1191G=
XM_006717910.2:c.*16G=	XP_006717973.1:n.*16G=
NM_001363518.1:c.*16G=	NP_001350447.1:n.*16G=
XM_017016377.2:c.*16G=	XP_016871866.1:n.*16G=
XM_017016378.2:c.*16G=	XP_016871867.1:n.*16G=
NM_018344.6:c.*16G= MANE Select	NP_060814.4:n.*16G=
NM_001174098.2:c.*673G=	NP_001167569.1:n.*673G=
NM_001363518.2:c.*16G=	NP_001350447.1:n.*16G=
NR_033413.2:n.1412G=
NR_033414.2:n.1185G=