Canonical Allele Identifier: CA1918678442

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362309A= , CM000672.2:g.71362309A=	GRCh38
NC_000010.10:g.73122066A= , CM000672.1:g.73122066A=	GRCh37
NC_000010.9:g.72792072A=	NCBI36
NG_017066.1:g.48057A=
NG_017066.2:g.48051A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2605A=
ENST00000373189.6:c.1129A= MANE Select	ENSP00000362285.5:p.Lys377=
ENST00000479577.2:c.895A=	ENSP00000493995.1:p.Lys299=
ENST00000642198.1:c.*701A=	ENSP00000494827.1:n.*701A=
ENST00000642772.1:c.*94+6066A=	ENSP00000495041.1:n.*94+6066A=
ENST00000643042.1:c.750A=	ENSP00000496674.1:n.750A=
ENST00000643619.1:c.*712A=	ENSP00000494378.1:n.*712A=
ENST00000643752.1:c.*455A=	ENSP00000495000.1:n.*455A=
ENST00000644088.1:c.*450A=	ENSP00000494066.1:n.*450A=
ENST00000644591.1:c.*455A=	ENSP00000496664.1:n.*455A=
ENST00000644895.1:c.*99+6066A=	ENSP00000493872.1:n.*99+6066A=
ENST00000645345.1:c.*701A=	ENSP00000495859.1:n.*701A=
ENST00000647524.1:c.*712A=	ENSP00000495077.1:n.*712A=
ENST00000373189.5:c.1129A=	ENSP00000362285.5:p.Lys377=
ENST00000469204.1:n.626A=
NM_001174098.1:c.*358A=	NP_001167569.1:n.*358A=
NM_018344.5:c.1129A=	NP_060814.4:p.Lys377=
NR_033413.1:n.1103A=
NR_033414.1:n.876A=
XM_006717910.2:c.895A=	XP_006717973.1:p.Lys299=
NM_001363518.1:c.895A=	NP_001350447.1:p.Lys299=
XM_017016377.2:c.691A=	XP_016871866.1:p.Lys231=
XM_017016378.2:c.511A=	XP_016871867.1:p.Lys171=
NM_018344.6:c.1129A= MANE Select	NP_060814.4:p.Lys377=
NM_001174098.2:c.*358A=	NP_001167569.1:n.*358A=
NM_001363518.2:c.895A=	NP_001350447.1:p.Lys299=
NR_033413.2:n.1097A=
NR_033414.2:n.870A=