Canonical Allele Identifier: CA1918678330

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362069C= , CM000672.2:g.71362069C=	GRCh38
NC_000010.10:g.73121826C= , CM000672.1:g.73121826C=	GRCh37
NC_000010.9:g.72791832C=	NCBI36
NG_017066.1:g.47817C=
NG_017066.2:g.47811C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2365C=
ENST00000373189.6:c.889C= MANE Select	ENSP00000362285.5:p.Pro297=
ENST00000479577.2:c.655C=	ENSP00000493995.1:p.Pro219=
ENST00000642198.1:c.*461C=	ENSP00000494827.1:n.*461C=
ENST00000642772.1:c.*94+5826C=	ENSP00000495041.1:n.*94+5826C=
ENST00000643042.1:c.510C=	ENSP00000496674.1:n.510C=
ENST00000643619.1:c.*472C=	ENSP00000494378.1:n.*472C=
ENST00000643752.1:c.*215C=	ENSP00000495000.1:n.*215C=
ENST00000644088.1:c.*210C=	ENSP00000494066.1:n.*210C=
ENST00000644591.1:c.*215C=	ENSP00000496664.1:n.*215C=
ENST00000644895.1:c.*99+5826C=	ENSP00000493872.1:n.*99+5826C=
ENST00000645345.1:c.*461C=	ENSP00000495859.1:n.*461C=
ENST00000647524.1:c.*472C=	ENSP00000495077.1:n.*472C=
ENST00000373189.5:c.889C=	ENSP00000362285.5:p.Pro297=
ENST00000469204.1:n.386C=
NM_001174098.1:c.*118C=	NP_001167569.1:n.*118C=
NM_018344.5:c.889C=	NP_060814.4:p.Pro297=
NR_033413.1:n.863C=
NR_033414.1:n.636C=
XM_006717910.2:c.655C=	XP_006717973.1:p.Pro219=
NM_001363518.1:c.655C=	NP_001350447.1:p.Pro219=
XM_017016377.2:c.451C=	XP_016871866.1:p.Pro151=
XM_017016378.2:c.271C=	XP_016871867.1:p.Pro91=
NM_018344.6:c.889C= MANE Select	NP_060814.4:p.Pro297=
NM_001174098.2:c.*118C=	NP_001167569.1:n.*118C=
NM_001363518.2:c.655C=	NP_001350447.1:p.Pro219=
NR_033413.2:n.857C=
NR_033414.2:n.630C=