Canonical Allele Identifier: CA470280986

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121828T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362071T>C , CM000672.2:g.71362071T>C	GRCh38
NC_000010.10:g.73121828T>C , CM000672.1:g.73121828T>C	GRCh37
NC_000010.9:g.72791834T>C	NCBI36
NG_017066.1:g.47819T>C
NG_017066.2:g.47813T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2367T>C
ENST00000373189.6:c.891T>C MANE Select	ENSP00000362285.5:p.Pro297=
ENST00000479577.2:c.657T>C	ENSP00000493995.1:p.Pro219=
ENST00000642198.1:c.*463T>C	ENSP00000494827.1:n.*463T>C
ENST00000642772.1:c.*94+5828T>C	ENSP00000495041.1:n.*94+5828T>C
ENST00000643042.1:c.512T>C	ENSP00000496674.1:n.512T>C
ENST00000643619.1:c.*474T>C	ENSP00000494378.1:n.*474T>C
ENST00000643752.1:c.*217T>C	ENSP00000495000.1:n.*217T>C
ENST00000644088.1:c.*212T>C	ENSP00000494066.1:n.*212T>C
ENST00000644591.1:c.*217T>C	ENSP00000496664.1:n.*217T>C
ENST00000644895.1:c.*99+5828T>C	ENSP00000493872.1:n.*99+5828T>C
ENST00000645345.1:c.*463T>C	ENSP00000495859.1:n.*463T>C
ENST00000647524.1:c.*474T>C	ENSP00000495077.1:n.*474T>C
ENST00000373189.5:c.891T>C	ENSP00000362285.5:p.Pro297=
ENST00000469204.1:n.388T>C
NM_001174098.1:c.*120T>C	NP_001167569.1:n.*120T>C
NM_018344.5:c.891T>C	NP_060814.4:p.Pro297=
NR_033413.1:n.865T>C
NR_033414.1:n.638T>C
XM_006717910.2:c.657T>C	XP_006717973.1:p.Pro219=
NM_001363518.1:c.657T>C	NP_001350447.1:p.Pro219=
XM_017016377.2:c.453T>C	XP_016871866.1:p.Pro151=
XM_017016378.2:c.273T>C	XP_016871867.1:p.Pro91=
NM_018344.6:c.891T>C MANE Select	NP_060814.4:p.Pro297=
NM_001174098.2:c.*120T>C	NP_001167569.1:n.*120T>C
NM_001363518.2:c.657T>C	NP_001350447.1:p.Pro219=
NR_033413.2:n.859T>C
NR_033414.2:n.632T>C