Canonical Allele Identifier: CA1918678345

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362099A= , CM000672.2:g.71362099A=	GRCh38
NC_000010.10:g.73121856A= , CM000672.1:g.73121856A=	GRCh37
NC_000010.9:g.72791862A=	NCBI36
NG_017066.1:g.47847A=
NG_017066.2:g.47841A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2395A=
ENST00000373189.6:c.919A= MANE Select	ENSP00000362285.5:p.Ser307=
ENST00000479577.2:c.685A=	ENSP00000493995.1:p.Ser229=
ENST00000642198.1:c.*491A=	ENSP00000494827.1:n.*491A=
ENST00000642772.1:c.*94+5856A=	ENSP00000495041.1:n.*94+5856A=
ENST00000643042.1:c.540A=	ENSP00000496674.1:n.540A=
ENST00000643619.1:c.*502A=	ENSP00000494378.1:n.*502A=
ENST00000643752.1:c.*245A=	ENSP00000495000.1:n.*245A=
ENST00000644088.1:c.*240A=	ENSP00000494066.1:n.*240A=
ENST00000644591.1:c.*245A=	ENSP00000496664.1:n.*245A=
ENST00000644895.1:c.*99+5856A=	ENSP00000493872.1:n.*99+5856A=
ENST00000645345.1:c.*491A=	ENSP00000495859.1:n.*491A=
ENST00000647524.1:c.*502A=	ENSP00000495077.1:n.*502A=
ENST00000373189.5:c.919A=	ENSP00000362285.5:p.Ser307=
ENST00000469204.1:n.416A=
NM_001174098.1:c.*148A=	NP_001167569.1:n.*148A=
NM_018344.5:c.919A=	NP_060814.4:p.Ser307=
NR_033413.1:n.893A=
NR_033414.1:n.666A=
XM_006717910.2:c.685A=	XP_006717973.1:p.Ser229=
NM_001363518.1:c.685A=	NP_001350447.1:p.Ser229=
XM_017016377.2:c.481A=	XP_016871866.1:p.Ser161=
XM_017016378.2:c.301A=	XP_016871867.1:p.Ser101=
NM_018344.6:c.919A= MANE Select	NP_060814.4:p.Ser307=
NM_001174098.2:c.*148A=	NP_001167569.1:n.*148A=
NM_001363518.2:c.685A=	NP_001350447.1:p.Ser229=
NR_033413.2:n.887A=
NR_033414.2:n.660A=