Canonical Allele Identifier: CA470281605

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122257T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362500T>C , CM000672.2:g.71362500T>C	GRCh38
NC_000010.10:g.73122257T>C , CM000672.1:g.73122257T>C	GRCh37
NC_000010.9:g.72792263T>C	NCBI36
NG_017066.1:g.48248T>C
NG_017066.2:g.48242T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2796T>C
ENST00000373189.6:c.1320T>C MANE Select	ENSP00000362285.5:p.Ile440=
ENST00000479577.2:c.1086T>C	ENSP00000493995.1:p.Ile362=
ENST00000642198.1:c.*892T>C	ENSP00000494827.1:n.*892T>C
ENST00000642772.1:c.*94+6257T>C	ENSP00000495041.1:n.*94+6257T>C
ENST00000643042.1:c.941T>C	ENSP00000496674.1:n.941T>C
ENST00000643619.1:c.*903T>C	ENSP00000494378.1:n.*903T>C
ENST00000643752.1:c.*646T>C	ENSP00000495000.1:n.*646T>C
ENST00000644088.1:c.*641T>C	ENSP00000494066.1:n.*641T>C
ENST00000644591.1:c.*646T>C	ENSP00000496664.1:n.*646T>C
ENST00000644895.1:c.*99+6257T>C	ENSP00000493872.1:n.*99+6257T>C
ENST00000645345.1:c.*892T>C	ENSP00000495859.1:n.*892T>C
ENST00000647524.1:c.*903T>C	ENSP00000495077.1:n.*903T>C
ENST00000373189.5:c.1320T>C	ENSP00000362285.5:p.Ile440=
ENST00000469204.1:n.817T>C
NM_001174098.1:c.*549T>C	NP_001167569.1:n.*549T>C
NM_018344.5:c.1320T>C	NP_060814.4:p.Ile440=
NR_033413.1:n.1294T>C
NR_033414.1:n.1067T>C
XM_006717910.2:c.1086T>C	XP_006717973.1:p.Ile362=
NM_001363518.1:c.1086T>C	NP_001350447.1:p.Ile362=
XM_017016377.2:c.882T>C	XP_016871866.1:p.Ile294=
XM_017016378.2:c.702T>C	XP_016871867.1:p.Ile234=
NM_018344.6:c.1320T>C MANE Select	NP_060814.4:p.Ile440=
NM_001174098.2:c.*549T>C	NP_001167569.1:n.*549T>C
NM_001363518.2:c.1086T>C	NP_001350447.1:p.Ile362=
NR_033413.2:n.1288T>C
NR_033414.2:n.1061T>C