Canonical Allele Identifier: CA1918678387

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362175C= , CM000672.2:g.71362175C=	GRCh38
NC_000010.10:g.73121932C= , CM000672.1:g.73121932C=	GRCh37
NC_000010.9:g.72791938C=	NCBI36
NG_017066.1:g.47923C=
NG_017066.2:g.47917C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2471C=
ENST00000373189.6:c.995C= MANE Select	ENSP00000362285.5:p.Ser332=
ENST00000479577.2:c.761C=	ENSP00000493995.1:p.Ser254=
ENST00000642198.1:c.*567C=	ENSP00000494827.1:n.*567C=
ENST00000642772.1:c.*94+5932C=	ENSP00000495041.1:n.*94+5932C=
ENST00000643042.1:c.616C=	ENSP00000496674.1:n.616C=
ENST00000643619.1:c.*578C=	ENSP00000494378.1:n.*578C=
ENST00000643752.1:c.*321C=	ENSP00000495000.1:n.*321C=
ENST00000644088.1:c.*316C=	ENSP00000494066.1:n.*316C=
ENST00000644591.1:c.*321C=	ENSP00000496664.1:n.*321C=
ENST00000644895.1:c.*99+5932C=	ENSP00000493872.1:n.*99+5932C=
ENST00000645345.1:c.*567C=	ENSP00000495859.1:n.*567C=
ENST00000647524.1:c.*578C=	ENSP00000495077.1:n.*578C=
ENST00000373189.5:c.995C=	ENSP00000362285.5:p.Ser332=
ENST00000469204.1:n.492C=
NM_001174098.1:c.*224C=	NP_001167569.1:n.*224C=
NM_018344.5:c.995C=	NP_060814.4:p.Ser332=
NR_033413.1:n.969C=
NR_033414.1:n.742C=
XM_006717910.2:c.761C=	XP_006717973.1:p.Ser254=
NM_001363518.1:c.761C=	NP_001350447.1:p.Ser254=
XM_017016377.2:c.557C=	XP_016871866.1:p.Ser186=
XM_017016378.2:c.377C=	XP_016871867.1:p.Ser126=
NM_018344.6:c.995C= MANE Select	NP_060814.4:p.Ser332=
NM_001174098.2:c.*224C=	NP_001167569.1:n.*224C=
NM_001363518.2:c.761C=	NP_001350447.1:p.Ser254=
NR_033413.2:n.963C=
NR_033414.2:n.736C=