Canonical Allele Identifier: CA1918678436

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362291G= , CM000672.2:g.71362291G=	GRCh38
NC_000010.10:g.73122048G= , CM000672.1:g.73122048G=	GRCh37
NC_000010.9:g.72792054G=	NCBI36
NG_017066.1:g.48039G=
NG_017066.2:g.48033G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697843.1:n.2587G=
ENST00000373189.6:c.1111G= MANE Select	ENSP00000362285.5:p.Val371=
ENST00000479577.2:c.877G=	ENSP00000493995.1:p.Val293=
ENST00000642198.1:c.*683G=	ENSP00000494827.1:n.*683G=
ENST00000642772.1:c.*94+6048G=	ENSP00000495041.1:n.*94+6048G=
ENST00000643042.1:c.732G=	ENSP00000496674.1:n.732G=
ENST00000643619.1:c.*694G=	ENSP00000494378.1:n.*694G=
ENST00000643752.1:c.*437G=	ENSP00000495000.1:n.*437G=
ENST00000644088.1:c.*432G=	ENSP00000494066.1:n.*432G=
ENST00000644591.1:c.*437G=	ENSP00000496664.1:n.*437G=
ENST00000644895.1:c.*99+6048G=	ENSP00000493872.1:n.*99+6048G=
ENST00000645345.1:c.*683G=	ENSP00000495859.1:n.*683G=
ENST00000647524.1:c.*694G=	ENSP00000495077.1:n.*694G=
ENST00000373189.5:c.1111G=	ENSP00000362285.5:p.Val371=
ENST00000469204.1:n.608G=
NM_001174098.1:c.*340G=	NP_001167569.1:n.*340G=
NM_018344.5:c.1111G=	NP_060814.4:p.Val371=
NR_033413.1:n.1085G=
NR_033414.1:n.858G=
XM_006717910.2:c.877G=	XP_006717973.1:p.Val293=
NM_001363518.1:c.877G=	NP_001350447.1:p.Val293=
XM_017016377.2:c.673G=	XP_016871866.1:p.Val225=
XM_017016378.2:c.493G=	XP_016871867.1:p.Val165=
NM_018344.6:c.1111G= MANE Select	NP_060814.4:p.Val371=
NM_001174098.2:c.*340G=	NP_001167569.1:n.*340G=
NM_001363518.2:c.877G=	NP_001350447.1:p.Val293=
NR_033413.2:n.1079G=
NR_033414.2:n.852G=