Canonical Allele Identifier: CA1918678441

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362308C= , CM000672.2:g.71362308C=	GRCh38
NC_000010.10:g.73122065C= , CM000672.1:g.73122065C=	GRCh37
NC_000010.9:g.72792071C=	NCBI36
NG_017066.1:g.48056C=
NG_017066.2:g.48050C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2604C=
ENST00000373189.6:c.1128C= MANE Select	ENSP00000362285.5:p.Ser376=
ENST00000479577.2:c.894C=	ENSP00000493995.1:p.Ser298=
ENST00000642198.1:c.*700C=	ENSP00000494827.1:n.*700C=
ENST00000642772.1:c.*94+6065C=	ENSP00000495041.1:n.*94+6065C=
ENST00000643042.1:c.749C=	ENSP00000496674.1:n.749C=
ENST00000643619.1:c.*711C=	ENSP00000494378.1:n.*711C=
ENST00000643752.1:c.*454C=	ENSP00000495000.1:n.*454C=
ENST00000644088.1:c.*449C=	ENSP00000494066.1:n.*449C=
ENST00000644591.1:c.*454C=	ENSP00000496664.1:n.*454C=
ENST00000644895.1:c.*99+6065C=	ENSP00000493872.1:n.*99+6065C=
ENST00000645345.1:c.*700C=	ENSP00000495859.1:n.*700C=
ENST00000647524.1:c.*711C=	ENSP00000495077.1:n.*711C=
ENST00000373189.5:c.1128C=	ENSP00000362285.5:p.Ser376=
ENST00000469204.1:n.625C=
NM_001174098.1:c.*357C=	NP_001167569.1:n.*357C=
NM_018344.5:c.1128C=	NP_060814.4:p.Ser376=
NR_033413.1:n.1102C=
NR_033414.1:n.875C=
XM_006717910.2:c.894C=	XP_006717973.1:p.Ser298=
NM_001363518.1:c.894C=	NP_001350447.1:p.Ser298=
XM_017016377.2:c.690C=	XP_016871866.1:p.Ser230=
XM_017016378.2:c.510C=	XP_016871867.1:p.Ser170=
NM_018344.6:c.1128C= MANE Select	NP_060814.4:p.Ser376=
NM_001174098.2:c.*357C=	NP_001167569.1:n.*357C=
NM_001363518.2:c.894C=	NP_001350447.1:p.Ser298=
NR_033413.2:n.1096C=
NR_033414.2:n.869C=