Canonical Allele Identifier: CA1918678399

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362195T= , CM000672.2:g.71362195T=	GRCh38
NC_000010.10:g.73121952T= , CM000672.1:g.73121952T=	GRCh37
NC_000010.9:g.72791958T=	NCBI36
NG_017066.1:g.47943T=
NG_017066.2:g.47937T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2491T=
ENST00000373189.6:c.1015T= MANE Select	ENSP00000362285.5:p.Ser339=
ENST00000479577.2:c.781T=	ENSP00000493995.1:p.Ser261=
ENST00000642198.1:c.*587T=	ENSP00000494827.1:n.*587T=
ENST00000642772.1:c.*94+5952T=	ENSP00000495041.1:n.*94+5952T=
ENST00000643042.1:c.636T=	ENSP00000496674.1:n.636T=
ENST00000643619.1:c.*598T=	ENSP00000494378.1:n.*598T=
ENST00000643752.1:c.*341T=	ENSP00000495000.1:n.*341T=
ENST00000644088.1:c.*336T=	ENSP00000494066.1:n.*336T=
ENST00000644591.1:c.*341T=	ENSP00000496664.1:n.*341T=
ENST00000644895.1:c.*99+5952T=	ENSP00000493872.1:n.*99+5952T=
ENST00000645345.1:c.*587T=	ENSP00000495859.1:n.*587T=
ENST00000647524.1:c.*598T=	ENSP00000495077.1:n.*598T=
ENST00000373189.5:c.1015T=	ENSP00000362285.5:p.Ser339=
ENST00000469204.1:n.512T=
NM_001174098.1:c.*244T=	NP_001167569.1:n.*244T=
NM_018344.5:c.1015T=	NP_060814.4:p.Ser339=
NR_033413.1:n.989T=
NR_033414.1:n.762T=
XM_006717910.2:c.781T=	XP_006717973.1:p.Ser261=
NM_001363518.1:c.781T=	NP_001350447.1:p.Ser261=
XM_017016377.2:c.577T=	XP_016871866.1:p.Ser193=
XM_017016378.2:c.397T=	XP_016871867.1:p.Ser133=
NM_018344.6:c.1015T= MANE Select	NP_060814.4:p.Ser339=
NM_001174098.2:c.*244T=	NP_001167569.1:n.*244T=
NM_001363518.2:c.781T=	NP_001350447.1:p.Ser261=
NR_033413.2:n.983T=
NR_033414.2:n.756T=