Canonical Allele Identifier: CA1918678311

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362034C= , CM000672.2:g.71362034C=	GRCh38
NC_000010.10:g.73121791C= , CM000672.1:g.73121791C=	GRCh37
NC_000010.9:g.72791797C=	NCBI36
NG_017066.1:g.47782C=
NG_017066.2:g.47776C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2330C=
ENST00000373189.6:c.854C= MANE Select	ENSP00000362285.5:p.Ser285=
ENST00000479577.2:c.620C=	ENSP00000493995.1:p.Ser207=
ENST00000642198.1:c.*426C=	ENSP00000494827.1:n.*426C=
ENST00000642772.1:c.*94+5791C=	ENSP00000495041.1:n.*94+5791C=
ENST00000643042.1:c.475C=	ENSP00000496674.1:n.475C=
ENST00000643619.1:c.*437C=	ENSP00000494378.1:n.*437C=
ENST00000643752.1:c.*180C=	ENSP00000495000.1:n.*180C=
ENST00000644088.1:c.*175C=	ENSP00000494066.1:n.*175C=
ENST00000644591.1:c.*180C=	ENSP00000496664.1:n.*180C=
ENST00000644895.1:c.*99+5791C=	ENSP00000493872.1:n.*99+5791C=
ENST00000645345.1:c.*426C=	ENSP00000495859.1:n.*426C=
ENST00000647524.1:c.*437C=	ENSP00000495077.1:n.*437C=
ENST00000373189.5:c.854C=	ENSP00000362285.5:p.Ser285=
ENST00000469204.1:n.351C=
NM_001174098.1:c.*83C=	NP_001167569.1:n.*83C=
NM_018344.5:c.854C=	NP_060814.4:p.Ser285=
NR_033413.1:n.828C=
NR_033414.1:n.601C=
XM_006717910.2:c.620C=	XP_006717973.1:p.Ser207=
NM_001363518.1:c.620C=	NP_001350447.1:p.Ser207=
XM_017016377.2:c.416C=	XP_016871866.1:p.Ser139=
XM_017016378.2:c.236C=	XP_016871867.1:p.Ser79=
NM_018344.6:c.854C= MANE Select	NP_060814.4:p.Ser285=
NM_001174098.2:c.*83C=	NP_001167569.1:n.*83C=
NM_001363518.2:c.620C=	NP_001350447.1:p.Ser207=
NR_033413.2:n.822C=
NR_033414.2:n.595C=