Canonical Allele Identifier: CA1918678532

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362488C= , CM000672.2:g.71362488C=	GRCh38
NC_000010.10:g.73122245C= , CM000672.1:g.73122245C=	GRCh37
NC_000010.9:g.72792251C=	NCBI36
NG_017066.1:g.48236C=
NG_017066.2:g.48230C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2784C=
ENST00000373189.6:c.1308C= MANE Select	ENSP00000362285.5:p.Tyr436=
ENST00000479577.2:c.1074C=	ENSP00000493995.1:p.Tyr358=
ENST00000642198.1:c.*880C=	ENSP00000494827.1:n.*880C=
ENST00000642772.1:c.*94+6245C=	ENSP00000495041.1:n.*94+6245C=
ENST00000643042.1:c.929C=	ENSP00000496674.1:n.929C=
ENST00000643619.1:c.*891C=	ENSP00000494378.1:n.*891C=
ENST00000643752.1:c.*634C=	ENSP00000495000.1:n.*634C=
ENST00000644088.1:c.*629C=	ENSP00000494066.1:n.*629C=
ENST00000644591.1:c.*634C=	ENSP00000496664.1:n.*634C=
ENST00000644895.1:c.*99+6245C=	ENSP00000493872.1:n.*99+6245C=
ENST00000645345.1:c.*880C=	ENSP00000495859.1:n.*880C=
ENST00000647524.1:c.*891C=	ENSP00000495077.1:n.*891C=
ENST00000373189.5:c.1308C=	ENSP00000362285.5:p.Tyr436=
ENST00000469204.1:n.805C=
NM_001174098.1:c.*537C=	NP_001167569.1:n.*537C=
NM_018344.5:c.1308C=	NP_060814.4:p.Tyr436=
NR_033413.1:n.1282C=
NR_033414.1:n.1055C=
XM_006717910.2:c.1074C=	XP_006717973.1:p.Tyr358=
NM_001363518.1:c.1074C=	NP_001350447.1:p.Tyr358=
XM_017016377.2:c.870C=	XP_016871866.1:p.Tyr290=
XM_017016378.2:c.690C=	XP_016871867.1:p.Tyr230=
NM_018344.6:c.1308C= MANE Select	NP_060814.4:p.Tyr436=
NM_001174098.2:c.*537C=	NP_001167569.1:n.*537C=
NM_001363518.2:c.1074C=	NP_001350447.1:p.Tyr358=
NR_033413.2:n.1276C=
NR_033414.2:n.1049C=