Canonical Allele Identifier: CA1918678495

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362412C= , CM000672.2:g.71362412C=	GRCh38
NC_000010.10:g.73122169C= , CM000672.1:g.73122169C=	GRCh37
NC_000010.9:g.72792175C=	NCBI36
NG_017066.1:g.48160C=
NG_017066.2:g.48154C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2708C=
ENST00000373189.6:c.1232C= MANE Select	ENSP00000362285.5:p.Ser411=
ENST00000479577.2:c.998C=	ENSP00000493995.1:p.Ser333=
ENST00000642198.1:c.*804C=	ENSP00000494827.1:n.*804C=
ENST00000642772.1:c.*94+6169C=	ENSP00000495041.1:n.*94+6169C=
ENST00000643042.1:c.853C=	ENSP00000496674.1:n.853C=
ENST00000643619.1:c.*815C=	ENSP00000494378.1:n.*815C=
ENST00000643752.1:c.*558C=	ENSP00000495000.1:n.*558C=
ENST00000644088.1:c.*553C=	ENSP00000494066.1:n.*553C=
ENST00000644591.1:c.*558C=	ENSP00000496664.1:n.*558C=
ENST00000644895.1:c.*99+6169C=	ENSP00000493872.1:n.*99+6169C=
ENST00000645345.1:c.*804C=	ENSP00000495859.1:n.*804C=
ENST00000647524.1:c.*815C=	ENSP00000495077.1:n.*815C=
ENST00000373189.5:c.1232C=	ENSP00000362285.5:p.Ser411=
ENST00000469204.1:n.729C=
NM_001174098.1:c.*461C=	NP_001167569.1:n.*461C=
NM_018344.5:c.1232C=	NP_060814.4:p.Ser411=
NR_033413.1:n.1206C=
NR_033414.1:n.979C=
XM_006717910.2:c.998C=	XP_006717973.1:p.Ser333=
NM_001363518.1:c.998C=	NP_001350447.1:p.Ser333=
XM_017016377.2:c.794C=	XP_016871866.1:p.Ser265=
XM_017016378.2:c.614C=	XP_016871867.1:p.Ser205=
NM_018344.6:c.1232C= MANE Select	NP_060814.4:p.Ser411=
NM_001174098.2:c.*461C=	NP_001167569.1:n.*461C=
NM_001363518.2:c.998C=	NP_001350447.1:p.Ser333=
NR_033413.2:n.1200C=
NR_033414.2:n.973C=