Canonical Allele Identifier: CA470281528

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122077A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362320A>C , CM000672.2:g.71362320A>C	GRCh38
NC_000010.10:g.73122077A>C , CM000672.1:g.73122077A>C	GRCh37
NC_000010.9:g.72792083A>C	NCBI36
NG_017066.1:g.48068A>C
NG_017066.2:g.48062A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2616A>C
ENST00000373189.6:c.1140A>C MANE Select	ENSP00000362285.5:p.Pro380=
ENST00000479577.2:c.906A>C	ENSP00000493995.1:p.Pro302=
ENST00000642198.1:c.*712A>C	ENSP00000494827.1:n.*712A>C
ENST00000642772.1:c.*94+6077A>C	ENSP00000495041.1:n.*94+6077A>C
ENST00000643042.1:c.761A>C	ENSP00000496674.1:n.761A>C
ENST00000643619.1:c.*723A>C	ENSP00000494378.1:n.*723A>C
ENST00000643752.1:c.*466A>C	ENSP00000495000.1:n.*466A>C
ENST00000644088.1:c.*461A>C	ENSP00000494066.1:n.*461A>C
ENST00000644591.1:c.*466A>C	ENSP00000496664.1:n.*466A>C
ENST00000644895.1:c.*99+6077A>C	ENSP00000493872.1:n.*99+6077A>C
ENST00000645345.1:c.*712A>C	ENSP00000495859.1:n.*712A>C
ENST00000647524.1:c.*723A>C	ENSP00000495077.1:n.*723A>C
ENST00000373189.5:c.1140A>C	ENSP00000362285.5:p.Pro380=
ENST00000469204.1:n.637A>C
NM_001174098.1:c.*369A>C	NP_001167569.1:n.*369A>C
NM_018344.5:c.1140A>C	NP_060814.4:p.Pro380=
NR_033413.1:n.1114A>C
NR_033414.1:n.887A>C
XM_006717910.2:c.906A>C	XP_006717973.1:p.Pro302=
NM_001363518.1:c.906A>C	NP_001350447.1:p.Pro302=
XM_017016377.2:c.702A>C	XP_016871866.1:p.Pro234=
XM_017016378.2:c.522A>C	XP_016871867.1:p.Pro174=
NM_018344.6:c.1140A>C MANE Select	NP_060814.4:p.Pro380=
NM_001174098.2:c.*369A>C	NP_001167569.1:n.*369A>C
NM_001363518.2:c.906A>C	NP_001350447.1:p.Pro302=
NR_033413.2:n.1108A>C
NR_033414.2:n.881A>C